Canonical Allele Identifier: CA1207936888
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1657670560
gnomAD v4: 1-173909530-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909530G>A , CM000663.2:g.173909530G>A GRCh38
NC_000001.10:g.173878668G>A , CM000663.1:g.173878668G>A GRCh37
NC_000001.9:g.172145291G>A NCBI36
NG_012462.1:g.12849C>T , LRG_577:g.12849C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1153+22C>T MANE Select ENSP00000356671.3:n.1153+22C>T
ENST00000367698.3:c.1153+22C>T ENSP00000356671.3:n.1153+22C>T
ENST00000617423.4:c.560-2037C>T ENSP00000478688.1:n.560-2037C>T
NM_000488.3:c.1153+22C>T , LRG_577t1:c.1153+22C>T NP_000479.1:n.1153+22C>T
XM_005245198.2:c.1009+22C>T XP_005245255.1:n.1009+22C>T
NM_001365052.1:c.1009+22C>T NP_001351981.1:n.1009+22C>T
NM_000488.4:c.1153+22C>T MANE Select NP_000479.1:n.1153+22C>T
NM_001365052.2:c.1009+22C>T NP_001351981.1:n.1009+22C>T
NM_001386302.1:c.1276+22C>T NP_001373231.1:n.1276+22C>T
NM_001386303.1:c.1234+22C>T NP_001373232.1:n.1234+22C>T
NM_001386304.1:c.1132+22C>T NP_001373233.1:n.1132+22C>T
NM_001386305.1:c.1096+22C>T NP_001373234.1:n.1096+22C>T
NM_001386306.1:c.937+22C>T NP_001373235.1:n.937+22C>T
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