Canonical Allele Identifier: CA337318329
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs377718335

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904087T>G , CM000685.2:g.154904087T>G GRCh38
NC_000023.10:g.154132362T>G , CM000685.1:g.154132362T>G GRCh37
NC_000023.9:g.153785556T>G NCBI36
NG_011403.1:g.123637A>C
NG_011403.2:g.123637A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5817A>C MANE Select ENSP00000353393.4:p.Ala1939=
ENST00000360256.8:c.5817A>C ENSP00000353393.4:p.Ala1939=
NM_000132.3:c.5817A>C NP_000123.1:p.Ala1939=
XM_011531126.1:c.5712A>C XP_011529428.1:p.Ala1904=
NM_000132.4:c.5817A>C MANE Select NP_000123.1:p.Ala1939=