Canonical Allele Identifier: CA10568180
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1800291

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154930010G>A , CM000685.2:g.154930010G>A GRCh38
NC_000023.10:g.154158285G>A , CM000685.1:g.154158285G>A GRCh37
NC_000023.9:g.153811479G>A NCBI36
NG_011403.1:g.97714C>T
NG_011403.2:g.97714C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.3780C>T MANE Select ENSP00000353393.4:p.Asp1260=
ENST00000360256.8:c.3780C>T ENSP00000353393.4:p.Asp1260=
NM_000132.3:c.3780C>T NP_000123.1:p.Asp1260=
XM_011531126.1:c.3675C>T XP_011529428.1:p.Asp1225=
NM_000132.4:c.3780C>T MANE Select NP_000123.1:p.Asp1260=