Canonical Allele Identifier: CA519358660
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs137852416
MyVariant Identifiers: chrX:g.154185348G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957073G>T , CM000685.2:g.154957073G>T GRCh38
NC_000023.10:g.154185348G>T , CM000685.1:g.154185348G>T GRCh37
NC_000023.9:g.153838542G>T NCBI36
NG_011403.1:g.70651C>A
NG_011403.2:g.70651C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1636C>A MANE Select ENSP00000353393.4:p.Arg546=
ENST00000647125.1:c.*1512C>A ENSP00000496062.1:n.*1512C>A
ENST00000360256.8:c.1636C>A ENSP00000353393.4:p.Arg546=
NM_000132.3:c.1636C>A NP_000123.1:p.Arg546=
XM_011531126.1:c.1531C>A XP_011529428.1:p.Arg511=
NM_000132.4:c.1636C>A MANE Select NP_000123.1:p.Arg546=