Canonical Allele Identifier: CA2579744489

Gene: F8

Linked Data

• gnomAD v4: X-154902195-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902195T>A , CM000685.2:g.154902195T>A	GRCh38
NC_000023.10:g.154130470T>A , CM000685.1:g.154130470T>A	GRCh37
NC_000023.9:g.153783664T>A	NCBI36
NG_011403.1:g.125529A>T
NG_011403.2:g.125529A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5999-28A>T MANE Select	ENSP00000353393.4:n.5999-28A>T
ENST00000360256.8:c.5999-28A>T	ENSP00000353393.4:n.5999-28A>T
NM_000132.3:c.5999-28A>T	NP_000123.1:n.5999-28A>T
XM_011531126.1:c.5894-28A>T	XP_011529428.1:n.5894-28A>T
NM_000132.4:c.5999-28A>T MANE Select	NP_000123.1:n.5999-28A>T