Canonical Allele Identifier: CA414914367
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154965990C>A , CM000685.2:g.154965990C>A GRCh38
NC_000023.10:g.154194265C>A , CM000685.1:g.154194265C>A GRCh37
NC_000023.9:g.153847459C>A NCBI36
NG_011403.1:g.61734G>T
NG_011403.2:g.61734G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1423G>T MANE Select ENSP00000353393.4:p.Glu475Ter
ENST00000647125.1:c.*1299G>T ENSP00000496062.1:n.*1299G>T
ENST00000360256.8:c.1423G>T ENSP00000353393.4:p.Glu475Ter
ENST00000483822.2:n.243G>T
NM_000132.3:c.1423G>T NP_000123.1:p.Glu475Ter
XM_011531126.1:c.1318G>T XP_011529428.1:p.Glu440Ter
NM_000132.4:c.1423G>T MANE Select NP_000123.1:p.Glu475Ter