Canonical Allele Identifier: CA343772092
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873052C>G (hg19) chr1:g.173903914C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903914C>G , CM000663.2:g.173903914C>G GRCh38
NC_000001.10:g.173873052C>G , CM000663.1:g.173873052C>G GRCh37
NC_000001.9:g.172139675C>G NCBI36
NG_012462.1:g.18465G>C , LRG_577:g.18465G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1370G>C MANE Select ENSP00000356671.3:p.Arg457Thr
ENST00000367698.3:c.1370G>C ENSP00000356671.3:p.Arg457Thr
ENST00000617423.4:c.755G>C ENSP00000478688.1:p.Arg252Thr
NM_000488.3:c.1370G>C , LRG_577t1:c.1370G>C NP_000479.1:p.Arg457Thr
XM_005245198.2:c.1226G>C XP_005245255.1:p.Arg409Thr
NM_001365052.1:c.1226G>C NP_001351981.1:p.Arg409Thr
NM_000488.4:c.1370G>C MANE Select NP_000479.1:p.Arg457Thr
NM_001365052.2:c.1226G>C NP_001351981.1:p.Arg409Thr
NM_001386302.1:c.1493G>C NP_001373231.1:p.Arg498Thr
NM_001386303.1:c.1451G>C NP_001373232.1:p.Arg484Thr
NM_001386304.1:c.1349G>C NP_001373233.1:p.Arg450Thr
NM_001386305.1:c.1313G>C NP_001373234.1:p.Arg438Thr
NM_001386306.1:c.1154G>C NP_001373235.1:p.Arg385Thr
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