Canonical Allele Identifier: CA421942758
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879000T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909862T>C , CM000663.2:g.173909862T>C GRCh38
NC_000001.10:g.173879000T>C , CM000663.1:g.173879000T>C GRCh37
NC_000001.9:g.172145623T>C NCBI36
NG_012462.1:g.12517A>G , LRG_577:g.12517A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.843A>G MANE Select ENSP00000356671.3:p.Ala281=
ENST00000367698.3:c.843A>G ENSP00000356671.3:p.Ala281=
ENST00000487183.1:n.494A>G
ENST00000617423.4:c.559+2002A>G ENSP00000478688.1:n.559+2002A>G
NM_000488.3:c.843A>G , LRG_577t1:c.843A>G NP_000479.1:p.Ala281=
XM_005245198.2:c.699A>G XP_005245255.1:p.Ala233=
NM_001365052.1:c.699A>G NP_001351981.1:p.Ala233=
NM_000488.4:c.843A>G MANE Select NP_000479.1:p.Ala281=
NM_001365052.2:c.699A>G NP_001351981.1:p.Ala233=
NM_001386302.1:c.966A>G NP_001373231.1:p.Ala322=
NM_001386303.1:c.924A>G NP_001373232.1:p.Ala308=
NM_001386304.1:c.822A>G NP_001373233.1:p.Ala274=
NM_001386305.1:c.786A>G NP_001373234.1:p.Ala262=
NM_001386306.1:c.627A>G NP_001373235.1:p.Ala209=
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