Canonical Allele Identifier: CA10567872
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782693200

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896199T>C , CM000685.2:g.154896199T>C GRCh38
NC_000023.10:g.154124474T>C , CM000685.1:g.154124474T>C GRCh37
NC_000023.9:g.153777668T>C NCBI36
NG_011403.1:g.131525A>G
NG_011403.2:g.131525A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6307A>G MANE Select ENSP00000353393.4:p.Ile2103Val
ENST00000360256.8:c.6307A>G ENSP00000353393.4:p.Ile2103Val
NM_000132.3:c.6307A>G NP_000123.1:p.Ile2103Val
XM_011531126.1:c.6202A>G XP_011529428.1:p.Ile2068Val
NM_000132.4:c.6307A>G MANE Select NP_000123.1:p.Ile2103Val