Canonical Allele Identifier: CA255022
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10115
dbSNP Id: rs28935203

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928694T>A , CM000685.2:g.154928694T>A GRCh38
NC_000023.10:g.154156969T>A , CM000685.1:g.154156969T>A GRCh37
NC_000023.9:g.153810163T>A NCBI36
NG_011403.1:g.99030A>T
NG_011403.2:g.99030A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5096A>T MANE Select ENSP00000353393.4:p.Tyr1699Phe
ENST00000360256.8:c.5096A>T ENSP00000353393.4:p.Tyr1699Phe
NM_000132.3:c.5096A>T NP_000123.1:p.Tyr1699Phe
XM_011531126.1:c.4991A>T XP_011529428.1:p.Tyr1664Phe
NM_000132.4:c.5096A>T MANE Select NP_000123.1:p.Tyr1699Phe