Canonical Allele Identifier: CA519352686
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154124427A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896152A>G , CM000685.2:g.154896152A>G GRCh38
NC_000023.10:g.154124427A>G , CM000685.1:g.154124427A>G GRCh37
NC_000023.9:g.153777621A>G NCBI36
NG_011403.1:g.131572T>C
NG_011403.2:g.131572T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6354T>C MANE Select ENSP00000353393.4:p.Ser2118=
ENST00000360256.8:c.6354T>C ENSP00000353393.4:p.Ser2118=
NM_000132.3:c.6354T>C NP_000123.1:p.Ser2118=
XM_011531126.1:c.6249T>C XP_011529428.1:p.Ser2083=
NM_000132.4:c.6354T>C MANE Select NP_000123.1:p.Ser2118=
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