Canonical Allele Identifier: CA414919905
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996990T>A , CM000685.2:g.154996990T>A GRCh38
NC_000023.10:g.154225265T>A , CM000685.1:g.154225265T>A GRCh37
NC_000023.9:g.153878459T>A NCBI36
NG_011403.1:g.30734A>T
NG_011403.2:g.30734A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.371A>T MANE Select ENSP00000353393.4:p.Tyr124Phe
ENST00000647125.1:c.*157A>T ENSP00000496062.1:n.*157A>T
ENST00000360256.8:c.371A>T ENSP00000353393.4:p.Tyr124Phe
ENST00000423959.5:c.266A>T ENSP00000409446.1:p.Tyr89Phe
ENST00000453950.1:c.353A>T ENSP00000389153.1:p.Tyr118Phe
NM_000132.3:c.371A>T NP_000123.1:p.Tyr124Phe
XM_011531126.1:c.266A>T XP_011529428.1:p.Tyr89Phe
NM_000132.4:c.371A>T MANE Select NP_000123.1:p.Tyr124Phe