Canonical Allele Identifier: CA10568599
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs781871471

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996996A>G , CM000685.2:g.154996996A>G GRCh38
NC_000023.10:g.154225271A>G , CM000685.1:g.154225271A>G GRCh37
NC_000023.9:g.153878465A>G NCBI36
NG_011403.1:g.30728T>C
NG_011403.2:g.30728T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.365T>C MANE Select ENSP00000353393.4:p.Val122Ala
ENST00000647125.1:c.*151T>C ENSP00000496062.1:n.*151T>C
ENST00000360256.8:c.365T>C ENSP00000353393.4:p.Val122Ala
ENST00000423959.5:c.260T>C ENSP00000409446.1:p.Val87Ala
ENST00000453950.1:c.347T>C ENSP00000389153.1:p.Val116Ala
NM_000132.3:c.365T>C NP_000123.1:p.Val122Ala
XM_011531126.1:c.260T>C XP_011529428.1:p.Val87Ala
NM_000132.4:c.365T>C MANE Select NP_000123.1:p.Val122Ala