Canonical Allele Identifier: CA421942787
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879033C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909895C>G , CM000663.2:g.173909895C>G GRCh38
NC_000001.10:g.173879033C>G , CM000663.1:g.173879033C>G GRCh37
NC_000001.9:g.172145656C>G NCBI36
NG_012462.1:g.12484G>C , LRG_577:g.12484G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.810G>C MANE Select ENSP00000356671.3:p.Leu270=
ENST00000367698.3:c.810G>C ENSP00000356671.3:p.Leu270=
ENST00000487183.1:n.461G>C
ENST00000617423.4:c.559+1969G>C ENSP00000478688.1:n.559+1969G>C
NM_000488.3:c.810G>C , LRG_577t1:c.810G>C NP_000479.1:p.Leu270=
XM_005245198.2:c.666G>C XP_005245255.1:p.Leu222=
NM_001365052.1:c.666G>C NP_001351981.1:p.Leu222=
NM_000488.4:c.810G>C MANE Select NP_000479.1:p.Leu270=
NM_001365052.2:c.666G>C NP_001351981.1:p.Leu222=
NM_001386302.1:c.933G>C NP_001373231.1:p.Leu311=
NM_001386303.1:c.891G>C NP_001373232.1:p.Leu297=
NM_001386304.1:c.789G>C NP_001373233.1:p.Leu263=
NM_001386305.1:c.763-10G>C NP_001373234.1:n.763-10G>C
NM_001386306.1:c.594G>C NP_001373235.1:p.Leu198=
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