Canonical Allele Identifier: CA414919894
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996986C>T , CM000685.2:g.154996986C>T GRCh38
NC_000023.10:g.154225261C>T , CM000685.1:g.154225261C>T GRCh37
NC_000023.9:g.153878455C>T NCBI36
NG_011403.1:g.30738G>A
NG_011403.2:g.30738G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.375G>A MANE Select ENSP00000353393.4:p.Trp125Ter
ENST00000647125.1:c.*161G>A ENSP00000496062.1:n.*161G>A
ENST00000360256.8:c.375G>A ENSP00000353393.4:p.Trp125Ter
ENST00000423959.5:c.270G>A ENSP00000409446.1:p.Trp90Ter
ENST00000453950.1:c.357G>A ENSP00000389153.1:p.Trp119Ter
NM_000132.3:c.375G>A NP_000123.1:p.Trp125Ter
XM_011531126.1:c.270G>A XP_011529428.1:p.Trp90Ter
NM_000132.4:c.375G>A MANE Select NP_000123.1:p.Trp125Ter