Canonical Allele Identifier: CA414914577
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928804C>A , CM000685.2:g.154928804C>A GRCh38
NC_000023.10:g.154157079C>A , CM000685.1:g.154157079C>A GRCh37
NC_000023.9:g.153810273C>A NCBI36
NG_011403.1:g.98920G>T
NG_011403.2:g.98920G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4986G>T MANE Select ENSP00000353393.4:p.Leu1662Phe
ENST00000360256.8:c.4986G>T ENSP00000353393.4:p.Leu1662Phe
NM_000132.3:c.4986G>T NP_000123.1:p.Leu1662Phe
XM_011531126.1:c.4881G>T XP_011529428.1:p.Leu1627Phe
NM_000132.4:c.4986G>T MANE Select NP_000123.1:p.Leu1662Phe