Canonical Allele Identifier: CA414920583

Gene: F8

Linked Data

• gnomAD v4: X-155022480-A-G
• MyVariant Identifiers: chrX:g.154250755A>G (hg19) ; chrX:g.155022480A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022480A>G , CM000685.2:g.155022480A>G	GRCh38
NC_000023.10:g.154250755A>G , CM000685.1:g.154250755A>G	GRCh37
NC_000023.9:g.153903949A>G	NCBI36
NG_011403.1:g.5244T>C
NG_011403.2:g.5244T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.73T>C MANE Select	ENSP00000353393.4:p.Tyr25His
ENST00000647125.1:c.73T>C	ENSP00000496062.1:p.Tyr25His
ENST00000360256.8:c.73T>C	ENSP00000353393.4:p.Tyr25His
ENST00000423959.5:c.38+4300T>C	ENSP00000409446.1:n.38+4300T>C
ENST00000453950.1:c.55T>C	ENSP00000389153.1:p.Tyr19His
NM_000132.3:c.73T>C	NP_000123.1:p.Tyr25His
XM_011531126.1:c.38+4300T>C	XP_011529428.1:n.38+4300T>C
NM_000132.4:c.73T>C MANE Select	NP_000123.1:p.Tyr25His