Canonical Allele Identifier: CA343773739
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878803A>C (hg19) chr1:g.173909665A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909665A>C , CM000663.2:g.173909665A>C GRCh38
NC_000001.10:g.173878803A>C , CM000663.1:g.173878803A>C GRCh37
NC_000001.9:g.172145426A>C NCBI36
NG_012462.1:g.12714T>G , LRG_577:g.12714T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1040T>G MANE Select ENSP00000356671.3:p.Met347Arg
ENST00000367698.3:c.1040T>G ENSP00000356671.3:p.Met347Arg
ENST00000617423.4:c.560-2172T>G ENSP00000478688.1:n.560-2172T>G
NM_000488.3:c.1040T>G , LRG_577t1:c.1040T>G NP_000479.1:p.Met347Arg
XM_005245198.2:c.896T>G XP_005245255.1:p.Met299Arg
NM_001365052.1:c.896T>G NP_001351981.1:p.Met299Arg
NM_000488.4:c.1040T>G MANE Select NP_000479.1:p.Met347Arg
NM_001365052.2:c.896T>G NP_001351981.1:p.Met299Arg
NM_001386302.1:c.1163T>G NP_001373231.1:p.Met388Arg
NM_001386303.1:c.1121T>G NP_001373232.1:p.Met374Arg
NM_001386304.1:c.1019T>G NP_001373233.1:p.Met340Arg
NM_001386305.1:c.983T>G NP_001373234.1:p.Met328Arg
NM_001386306.1:c.824T>G NP_001373235.1:p.Met275Arg
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