Canonical Allele Identifier: CA337336042

Gene: F8

Linked Data

• dbSNP Id: rs782791657
• gnomAD v3: X-154965902-A-T
• gnomAD v4: X-154965902-A-T
• MyVariant Identifiers: chrX:g.154194177A>T (hg19) ; chrX:g.154965902A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154965902A>T , CM000685.2:g.154965902A>T	GRCh38
NC_000023.10:g.154194177A>T , CM000685.1:g.154194177A>T	GRCh37
NC_000023.9:g.153847371A>T	NCBI36
NG_011403.1:g.61822T>A
NG_011403.2:g.61822T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1443+68T>A MANE Select	ENSP00000353393.4:n.1443+68T>A
ENST00000647125.1:c.*1319+68T>A	ENSP00000496062.1:n.*1319+68T>A
ENST00000360256.8:c.1443+68T>A	ENSP00000353393.4:n.1443+68T>A
ENST00000483822.2:n.331T>A
NM_000132.3:c.1443+68T>A	NP_000123.1:n.1443+68T>A
XM_011531126.1:c.1338+68T>A	XP_011529428.1:n.1338+68T>A
NM_000132.4:c.1443+68T>A MANE Select	NP_000123.1:n.1443+68T>A