Canonical Allele Identifier: CA414910268
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953899G>C , CM000685.2:g.154953899G>C GRCh38
NC_000023.10:g.154182174G>C , CM000685.1:g.154182174G>C GRCh37
NC_000023.9:g.153835368G>C NCBI36
NG_011403.1:g.73825C>G
NG_011403.2:g.73825C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1896C>G MANE Select ENSP00000353393.4:p.Ile632Met
ENST00000647125.1:c.*1772C>G ENSP00000496062.1:n.*1772C>G
ENST00000360256.8:c.1896C>G ENSP00000353393.4:p.Ile632Met
NM_000132.3:c.1896C>G NP_000123.1:p.Ile632Met
XM_011531126.1:c.1791C>G XP_011529428.1:p.Ile597Met
NM_000132.4:c.1896C>G MANE Select NP_000123.1:p.Ile632Met