Canonical Allele Identifier: CA10568604

Gene: F8

Linked Data

• dbSNP Id: rs782680109
• ExAC: X:154225369 A / G
• gnomAD v2: X-154225369-A-G
• gnomAD v4: X-154997094-A-G
• MyVariant Identifiers: chrX:g.154225369A>G (hg19) ; chrX:g.154997094A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997094A>G , CM000685.2:g.154997094A>G	GRCh38
NC_000023.10:g.154225369A>G , CM000685.1:g.154225369A>G	GRCh37
NC_000023.9:g.153878563A>G	NCBI36
NG_011403.1:g.30630T>C
NG_011403.2:g.30630T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.267T>C MANE Select	ENSP00000353393.4:p.Gly89=
ENST00000647125.1:c.*53T>C	ENSP00000496062.1:n.*53T>C
ENST00000360256.8:c.267T>C	ENSP00000353393.4:p.Gly89=
ENST00000423959.5:c.162T>C	ENSP00000409446.1:p.Gly54=
ENST00000453950.1:c.249T>C	ENSP00000389153.1:p.Gly83=
NM_000132.3:c.267T>C	NP_000123.1:p.Gly89=
XM_011531126.1:c.162T>C	XP_011529428.1:p.Gly54=
NM_000132.4:c.267T>C MANE Select	NP_000123.1:p.Gly89=