Canonical Allele Identifier: CA337346842

Gene: F8

Linked Data

• dbSNP Id: rs782445164
• gnomAD v3: X-154993531-C-A
• gnomAD v4: X-154993531-C-A
• MyVariant Identifiers: chrX:g.154221806C>A (hg19) ; chrX:g.154993531C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993531C>A , CM000685.2:g.154993531C>A	GRCh38
NC_000023.10:g.154221806C>A , CM000685.1:g.154221806C>A	GRCh37
NC_000023.9:g.153875000C>A	NCBI36
NG_011403.1:g.34193G>T
NG_011403.2:g.34193G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.389-383G>T MANE Select	ENSP00000353393.4:n.389-383G>T
ENST00000647125.1:c.*175-383G>T	ENSP00000496062.1:n.*175-383G>T
ENST00000360256.8:c.389-383G>T	ENSP00000353393.4:n.389-383G>T
ENST00000423959.5:c.284-383G>T	ENSP00000409446.1:n.284-383G>T
ENST00000453950.1:c.371-383G>T	ENSP00000389153.1:n.371-383G>T
NM_000132.3:c.389-383G>T	NP_000123.1:n.389-383G>T
XM_011531126.1:c.284-383G>T	XP_011529428.1:n.284-383G>T
NM_000132.4:c.389-383G>T MANE Select	NP_000123.1:n.389-383G>T