Canonical Allele Identifier: CA873354157

Gene: F8

Linked Data

• dbSNP Id: rs1206639819
• gnomAD v3: X-154957358-G-A
• gnomAD v4: X-154957358-G-A
• MyVariant Identifiers: chrX:g.154957358G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957358G>A , CM000685.2:g.154957358G>A	GRCh38
NC_000023.10:g.154185633G>A , CM000685.1:g.154185633G>A	GRCh37
NC_000023.9:g.153838827G>A	NCBI36
NG_011403.1:g.70366C>T
NG_011403.2:g.70366C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1538-187C>T MANE Select	ENSP00000353393.4:n.1538-187C>T
ENST00000647125.1:c.*1414-187C>T	ENSP00000496062.1:n.*1414-187C>T
ENST00000360256.8:c.1538-187C>T	ENSP00000353393.4:n.1538-187C>T
NM_000132.3:c.1538-187C>T	NP_000123.1:n.1538-187C>T
XM_011531126.1:c.1433-187C>T	XP_011529428.1:n.1433-187C>T
NM_000132.4:c.1538-187C>T MANE Select	NP_000123.1:n.1538-187C>T