Canonical Allele Identifier: CA343772681
Gene: SERPINC1 HGNC NCBI

Linked Data

gnomAD v4: 1-173904056-C-G
MyVariant Identifiers: chr1:g.173873194C>G (hg19) chr1:g.173904056C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904056C>G , CM000663.2:g.173904056C>G GRCh38
NC_000001.10:g.173873194C>G , CM000663.1:g.173873194C>G GRCh37
NC_000001.9:g.172139817C>G NCBI36
NG_012462.1:g.18323G>C , LRG_577:g.18323G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1228G>C MANE Select ENSP00000356671.3:p.Glu410Gln
ENST00000367698.3:c.1228G>C ENSP00000356671.3:p.Glu410Gln
ENST00000617423.4:c.613G>C ENSP00000478688.1:p.Glu205Gln
NM_000488.3:c.1228G>C , LRG_577t1:c.1228G>C NP_000479.1:p.Glu410Gln
XM_005245198.2:c.1084G>C XP_005245255.1:p.Glu362Gln
NM_001365052.1:c.1084G>C NP_001351981.1:p.Glu362Gln
NM_000488.4:c.1228G>C MANE Select NP_000479.1:p.Glu410Gln
NM_001365052.2:c.1084G>C NP_001351981.1:p.Glu362Gln
NM_001386302.1:c.1351G>C NP_001373231.1:p.Glu451Gln
NM_001386303.1:c.1309G>C NP_001373232.1:p.Glu437Gln
NM_001386304.1:c.1207G>C NP_001373233.1:p.Glu403Gln
NM_001386305.1:c.1171G>C NP_001373234.1:p.Glu391Gln
NM_001386306.1:c.1012G>C NP_001373235.1:p.Glu338Gln
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