Canonical Allele Identifier: CA343774428
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878969A>C (hg19) chr1:g.173909831A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909831A>C , CM000663.2:g.173909831A>C GRCh38
NC_000001.10:g.173878969A>C , CM000663.1:g.173878969A>C GRCh37
NC_000001.9:g.172145592A>C NCBI36
NG_012462.1:g.12548T>G , LRG_577:g.12548T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.874T>G MANE Select ENSP00000356671.3:p.Tyr292Asp
ENST00000367698.3:c.874T>G ENSP00000356671.3:p.Tyr292Asp
ENST00000487183.1:n.525T>G
ENST00000617423.4:c.559+2033T>G ENSP00000478688.1:n.559+2033T>G
NM_000488.3:c.874T>G , LRG_577t1:c.874T>G NP_000479.1:p.Tyr292Asp
XM_005245198.2:c.730T>G XP_005245255.1:p.Tyr244Asp
NM_001365052.1:c.730T>G NP_001351981.1:p.Tyr244Asp
NM_000488.4:c.874T>G MANE Select NP_000479.1:p.Tyr292Asp
NM_001365052.2:c.730T>G NP_001351981.1:p.Tyr244Asp
NM_001386302.1:c.997T>G NP_001373231.1:p.Tyr333Asp
NM_001386303.1:c.955T>G NP_001373232.1:p.Tyr319Asp
NM_001386304.1:c.853T>G NP_001373233.1:p.Tyr285Asp
NM_001386305.1:c.817T>G NP_001373234.1:p.Tyr273Asp
NM_001386306.1:c.658T>G NP_001373235.1:p.Tyr220Asp
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