Canonical Allele Identifier: CA414919982
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1803284
dbSNP Id: rs2073620915

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997026G>A , CM000685.2:g.154997026G>A GRCh38
NC_000023.10:g.154225301G>A , CM000685.1:g.154225301G>A GRCh37
NC_000023.9:g.153878495G>A NCBI36
NG_011403.1:g.30698C>T
NG_011403.2:g.30698C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.335C>T MANE Select ENSP00000353393.4:p.Ser112Phe
ENST00000647125.1:c.*121C>T ENSP00000496062.1:n.*121C>T
ENST00000360256.8:c.335C>T ENSP00000353393.4:p.Ser112Phe
ENST00000423959.5:c.230C>T ENSP00000409446.1:p.Ser77Phe
ENST00000453950.1:c.317C>T ENSP00000389153.1:p.Ser106Phe
NM_000132.3:c.335C>T NP_000123.1:p.Ser112Phe
XM_011531126.1:c.230C>T XP_011529428.1:p.Ser77Phe
NM_000132.4:c.335C>T MANE Select NP_000123.1:p.Ser112Phe