Canonical Allele Identifier: CA10567877

Gene: F8

Linked Data

• dbSNP Id: rs782471646
• ExAC: X:154124512 C / G
• gnomAD v2: X-154124512-C-G
• gnomAD v4: X-154896237-C-G
• MyVariant Identifiers: chrX:g.154124512C>G (hg19) ; chrX:g.154896237C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896237C>G , CM000685.2:g.154896237C>G	GRCh38
NC_000023.10:g.154124512C>G , CM000685.1:g.154124512C>G	GRCh37
NC_000023.9:g.153777706C>G	NCBI36
NG_011403.1:g.131487G>C
NG_011403.2:g.131487G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6274-5G>C MANE Select	ENSP00000353393.4:n.6274-5G>C
ENST00000360256.8:c.6274-5G>C	ENSP00000353393.4:n.6274-5G>C
NM_000132.3:c.6274-5G>C	NP_000123.1:n.6274-5G>C
XM_011531126.1:c.6169-5G>C	XP_011529428.1:n.6169-5G>C
NM_000132.4:c.6274-5G>C MANE Select	NP_000123.1:n.6274-5G>C