Canonical Allele Identifier: CA414908738
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904920A>G , CM000685.2:g.154904920A>G GRCh38
NC_000023.10:g.154133195A>G , CM000685.1:g.154133195A>G GRCh37
NC_000023.9:g.153786389A>G NCBI36
NG_011403.1:g.122804T>C
NG_011403.2:g.122804T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5477T>C MANE Select ENSP00000353393.4:p.Val1826Ala
ENST00000360256.8:c.5477T>C ENSP00000353393.4:p.Val1826Ala
NM_000132.3:c.5477T>C NP_000123.1:p.Val1826Ala
XM_011531126.1:c.5372T>C XP_011529428.1:p.Val1791Ala
NM_000132.4:c.5477T>C MANE Select NP_000123.1:p.Val1826Ala