Canonical Allele Identifier: CA10568411

Gene: F8

Linked Data

• dbSNP Id: rs782437818
• ExAC: X:154185189 A / T
• gnomAD v4: X-154956914-A-T
• MyVariant Identifiers: chrX:g.154185189A>T (hg19) ; chrX:g.154956914A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154956914A>T , CM000685.2:g.154956914A>T	GRCh38
NC_000023.10:g.154185189A>T , CM000685.1:g.154185189A>T	GRCh37
NC_000023.9:g.153838383A>T	NCBI36
NG_011403.1:g.70810T>A
NG_011403.2:g.70810T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1752+43T>A MANE Select	ENSP00000353393.4:n.1752+43T>A
ENST00000647125.1:c.*1628+43T>A	ENSP00000496062.1:n.*1628+43T>A
ENST00000360256.8:c.1752+43T>A	ENSP00000353393.4:n.1752+43T>A
NM_000132.3:c.1752+43T>A	NP_000123.1:n.1752+43T>A
XM_011531126.1:c.1647+43T>A	XP_011529428.1:n.1647+43T>A
NM_000132.4:c.1752+43T>A MANE Select	NP_000123.1:n.1752+43T>A