Canonical Allele Identifier: CA414920084

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225347C>T (hg19) ; chrX:g.154997072C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997072C>T , CM000685.2:g.154997072C>T	GRCh38
NC_000023.10:g.154225347C>T , CM000685.1:g.154225347C>T	GRCh37
NC_000023.9:g.153878541C>T	NCBI36
NG_011403.1:g.30652G>A
NG_011403.2:g.30652G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.289G>A MANE Select	ENSP00000353393.4:p.Ala97Thr
ENST00000647125.1:c.*75G>A	ENSP00000496062.1:n.*75G>A
ENST00000360256.8:c.289G>A	ENSP00000353393.4:p.Ala97Thr
ENST00000423959.5:c.184G>A	ENSP00000409446.1:p.Ala62Thr
ENST00000453950.1:c.271G>A	ENSP00000389153.1:p.Ala91Thr
NM_000132.3:c.289G>A	NP_000123.1:p.Ala97Thr
XM_011531126.1:c.184G>A	XP_011529428.1:p.Ala62Thr
NM_000132.4:c.289G>A MANE Select	NP_000123.1:p.Ala97Thr