Canonical Allele Identifier: CA873356344

Gene: F8

Linked Data

• dbSNP Id: rs1202348570
• gnomAD v3: X-154993398-G-C
• gnomAD v4: X-154993398-G-C
• MyVariant Identifiers: chrX:g.154993398G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993398G>C , CM000685.2:g.154993398G>C	GRCh38
NC_000023.10:g.154221673G>C , CM000685.1:g.154221673G>C	GRCh37
NC_000023.9:g.153874867G>C	NCBI36
NG_011403.1:g.34326C>G
NG_011403.2:g.34326C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.389-250C>G MANE Select	ENSP00000353393.4:n.389-250C>G
ENST00000647125.1:c.*175-250C>G	ENSP00000496062.1:n.*175-250C>G
ENST00000360256.8:c.389-250C>G	ENSP00000353393.4:n.389-250C>G
ENST00000423959.5:c.284-250C>G	ENSP00000409446.1:n.284-250C>G
ENST00000453950.1:c.371-250C>G	ENSP00000389153.1:n.371-250C>G
NM_000132.3:c.389-250C>G	NP_000123.1:n.389-250C>G
XM_011531126.1:c.284-250C>G	XP_011529428.1:n.284-250C>G
NM_000132.4:c.389-250C>G MANE Select	NP_000123.1:n.389-250C>G