Canonical Allele Identifier: CA2695169097
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154954158T>A , CM000685.2:g.154954158T>A GRCh38
NC_000023.10:g.154182433T>A , CM000685.1:g.154182433T>A GRCh37
NC_000023.9:g.153835627T>A NCBI36
NG_011403.1:g.73566A>T
NG_011403.2:g.73566A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1753-116A>T MANE Select ENSP00000353393.4:n.1753-116A>T
ENST00000647125.1:c.*1629-116A>T ENSP00000496062.1:n.*1629-116A>T
ENST00000360256.8:c.1753-116A>T ENSP00000353393.4:n.1753-116A>T
NM_000132.3:c.1753-116A>T NP_000123.1:n.1753-116A>T
XM_011531126.1:c.1648-116A>T XP_011529428.1:n.1648-116A>T
NM_000132.4:c.1753-116A>T MANE Select NP_000123.1:n.1753-116A>T