Canonical Allele Identifier: CA414919610

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154221326C>A (hg19) ; chrX:g.154993051C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993051C>A , CM000685.2:g.154993051C>A	GRCh38
NC_000023.10:g.154221326C>A , CM000685.1:g.154221326C>A	GRCh37
NC_000023.9:g.153874520C>A	NCBI36
NG_011403.1:g.34673G>T
NG_011403.2:g.34673G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.486G>T MANE Select	ENSP00000353393.4:p.Glu162Asp
ENST00000647125.1:c.*272G>T	ENSP00000496062.1:n.*272G>T
ENST00000360256.8:c.486G>T	ENSP00000353393.4:p.Glu162Asp
ENST00000423959.5:c.381G>T	ENSP00000409446.1:p.Glu127Asp
ENST00000453950.1:c.468G>T	ENSP00000389153.1:p.Glu156Asp
NM_000132.3:c.486G>T	NP_000123.1:p.Glu162Asp
XM_011531126.1:c.381G>T	XP_011529428.1:p.Glu127Asp
NM_000132.4:c.486G>T MANE Select	NP_000123.1:p.Glu162Asp