Canonical Allele Identifier: CA414919924
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996999C>T , CM000685.2:g.154996999C>T GRCh38
NC_000023.10:g.154225274C>T , CM000685.1:g.154225274C>T GRCh37
NC_000023.9:g.153878468C>T NCBI36
NG_011403.1:g.30725G>A
NG_011403.2:g.30725G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.362G>A MANE Select ENSP00000353393.4:p.Gly121Asp
ENST00000647125.1:c.*148G>A ENSP00000496062.1:n.*148G>A
ENST00000360256.8:c.362G>A ENSP00000353393.4:p.Gly121Asp
ENST00000423959.5:c.257G>A ENSP00000409446.1:p.Gly86Asp
ENST00000453950.1:c.344G>A ENSP00000389153.1:p.Gly115Asp
NM_000132.3:c.362G>A NP_000123.1:p.Gly121Asp
XM_011531126.1:c.257G>A XP_011529428.1:p.Gly86Asp
NM_000132.4:c.362G>A MANE Select NP_000123.1:p.Gly121Asp