Canonical Allele Identifier: CA414920012
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997039T>A , CM000685.2:g.154997039T>A GRCh38
NC_000023.10:g.154225314T>A , CM000685.1:g.154225314T>A GRCh37
NC_000023.9:g.153878508T>A NCBI36
NG_011403.1:g.30685A>T
NG_011403.2:g.30685A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.322A>T MANE Select ENSP00000353393.4:p.Lys108Ter
ENST00000647125.1:c.*108A>T ENSP00000496062.1:n.*108A>T
ENST00000360256.8:c.322A>T ENSP00000353393.4:p.Lys108Ter
ENST00000423959.5:c.217A>T ENSP00000409446.1:p.Lys73Ter
ENST00000453950.1:c.304A>T ENSP00000389153.1:p.Lys102Ter
NM_000132.3:c.322A>T NP_000123.1:p.Lys108Ter
XM_011531126.1:c.217A>T XP_011529428.1:p.Lys73Ter
NM_000132.4:c.322A>T MANE Select NP_000123.1:p.Lys108Ter