Canonical Allele Identifier: CA414899868
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896163G>A , CM000685.2:g.154896163G>A GRCh38
NC_000023.10:g.154124438G>A , CM000685.1:g.154124438G>A GRCh37
NC_000023.9:g.153777632G>A NCBI36
NG_011403.1:g.131561C>T
NG_011403.2:g.131561C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6343C>T MANE Select ENSP00000353393.4:p.Leu2115Phe
ENST00000360256.8:c.6343C>T ENSP00000353393.4:p.Leu2115Phe
NM_000132.3:c.6343C>T NP_000123.1:p.Leu2115Phe
XM_011531126.1:c.6238C>T XP_011529428.1:p.Leu2080Phe
NM_000132.4:c.6343C>T MANE Select NP_000123.1:p.Leu2115Phe