Canonical Allele Identifier: CA10567869
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782385047

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896175T>C , CM000685.2:g.154896175T>C GRCh38
NC_000023.10:g.154124450T>C , CM000685.1:g.154124450T>C GRCh37
NC_000023.9:g.153777644T>C NCBI36
NG_011403.1:g.131549A>G
NG_011403.2:g.131549A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6331A>G MANE Select ENSP00000353393.4:p.Lys2111Glu
ENST00000360256.8:c.6331A>G ENSP00000353393.4:p.Lys2111Glu
NM_000132.3:c.6331A>G NP_000123.1:p.Lys2111Glu
XM_011531126.1:c.6226A>G XP_011529428.1:p.Lys2076Glu
NM_000132.4:c.6331A>G MANE Select NP_000123.1:p.Lys2111Glu