Canonical Allele Identifier: CA414902134

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154159715C>A (hg19) ; chrX:g.154931440C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154931440C>A , CM000685.2:g.154931440C>A	GRCh38
NC_000023.10:g.154159715C>A , CM000685.1:g.154159715C>A	GRCh37
NC_000023.9:g.153812909C>A	NCBI36
NG_011403.1:g.96284G>T
NG_011403.2:g.96284G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.2350G>T MANE Select	ENSP00000353393.4:p.Asp784Tyr
ENST00000647125.1:c.*2016G>T	ENSP00000496062.1:n.*2016G>T
ENST00000360256.8:c.2350G>T	ENSP00000353393.4:p.Asp784Tyr
NM_000132.3:c.2350G>T	NP_000123.1:p.Asp784Tyr
XM_011531126.1:c.2245G>T	XP_011529428.1:p.Asp749Tyr
NM_000132.4:c.2350G>T MANE Select	NP_000123.1:p.Asp784Tyr