Canonical Allele Identifier: CA414896919

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065925G>T (hg19) ; chrX:g.154837650G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837650G>T , CM000685.2:g.154837650G>T	GRCh38
NC_000023.10:g.154065925G>T , CM000685.1:g.154065925G>T	GRCh37
NC_000023.9:g.153719119G>T	NCBI36
NG_011403.1:g.190074C>A
NG_033065.1:g.2013C>A
NG_011403.2:g.190074C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7003C>A MANE Select	ENSP00000353393.4:p.Gln2335Lys
ENST00000644698.1:c.736C>A	ENSP00000495706.1:p.Gln246Lys
ENST00000330287.10:c.598C>A	ENSP00000327895.6:p.Gln200Lys
ENST00000360256.8:c.7003C>A	ENSP00000353393.4:p.Gln2335Lys
NM_000132.3:c.7003C>A	NP_000123.1:p.Gln2335Lys
NM_019863.2:c.598C>A	NP_063916.1:p.Gln200Lys
XM_011531126.1:c.6898C>A	XP_011529428.1:p.Gln2300Lys
NM_000132.4:c.7003C>A MANE Select	NP_000123.1:p.Gln2335Lys
NM_019863.3:c.598C>A	NP_063916.1:p.Gln200Lys