Canonical Allele Identifier: CA414905382

Gene: F8

Linked Data

• dbSNP Id: rs1433499371
• MyVariant Identifiers: chrX:g.154132179A>G (hg19) ; chrX:g.154903904A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903904A>G , CM000685.2:g.154903904A>G	GRCh38
NC_000023.10:g.154132179A>G , CM000685.1:g.154132179A>G	GRCh37
NC_000023.9:g.153785373A>G	NCBI36
NG_011403.1:g.123820T>C
NG_011403.2:g.123820T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.5998+2T>C MANE Select	ENSP00000353393.4:n.5998+2T>C
ENST00000360256.8:c.5998+2T>C	ENSP00000353393.4:n.5998+2T>C
NM_000132.3:c.5998+2T>C	NP_000123.1:n.5998+2T>C
XM_011531126.1:c.5893+2T>C	XP_011529428.1:n.5893+2T>C
NM_000132.4:c.5998+2T>C MANE Select	NP_000123.1:n.5998+2T>C