Canonical Allele Identifier: CA414914457

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154194282C>G (hg19) ; chrX:g.154966007C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154966007C>G , CM000685.2:g.154966007C>G	GRCh38
NC_000023.10:g.154194282C>G , CM000685.1:g.154194282C>G	GRCh37
NC_000023.9:g.153847476C>G	NCBI36
NG_011403.1:g.61717G>C
NG_011403.2:g.61717G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1406G>C MANE Select	ENSP00000353393.4:p.Gly469Ala
ENST00000647125.1:c.*1282G>C	ENSP00000496062.1:n.*1282G>C
ENST00000360256.8:c.1406G>C	ENSP00000353393.4:p.Gly469Ala
ENST00000483822.2:n.226G>C
NM_000132.3:c.1406G>C	NP_000123.1:p.Gly469Ala
XM_011531126.1:c.1301G>C	XP_011529428.1:p.Gly434Ala
NM_000132.4:c.1406G>C MANE Select	NP_000123.1:p.Gly469Ala