Canonical Allele Identifier: CA414919901
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996988A>G , CM000685.2:g.154996988A>G GRCh38
NC_000023.10:g.154225263A>G , CM000685.1:g.154225263A>G GRCh37
NC_000023.9:g.153878457A>G NCBI36
NG_011403.1:g.30736T>C
NG_011403.2:g.30736T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.373T>C MANE Select ENSP00000353393.4:p.Trp125Arg
ENST00000647125.1:c.*159T>C ENSP00000496062.1:n.*159T>C
ENST00000360256.8:c.373T>C ENSP00000353393.4:p.Trp125Arg
ENST00000423959.5:c.268T>C ENSP00000409446.1:p.Trp90Arg
ENST00000453950.1:c.355T>C ENSP00000389153.1:p.Trp119Arg
NM_000132.3:c.373T>C NP_000123.1:p.Trp125Arg
XM_011531126.1:c.268T>C XP_011529428.1:p.Trp90Arg
NM_000132.4:c.373T>C MANE Select NP_000123.1:p.Trp125Arg