Canonical Allele Identifier: CA255201
Gene: F8 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 10308
ClinVar RCV Id: RCV000011021
dbSNP Id: rs137852457

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896228T>C , CM000685.2:g.154896228T>C GRCh38
NC_000023.10:g.154124503T>C , CM000685.1:g.154124503T>C GRCh37
NC_000023.9:g.153777697T>C NCBI36
NG_011403.1:g.131496A>G

Transcript Alleles

HGVS Amino-acid change
NM_000132.3:c.6278A>G VV NP_000123.1:p.Asp2093Gly
XM_011531126.1:c.6173A>G XP_011529428.1:p.Asp2058Gly
ENST00000360256.8:c.6278A>G ENSP00000353393.4:p.Asp2093Gly