Canonical Allele Identifier: CA414919608

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154221325T>C (hg19) ; chrX:g.154993050T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993050T>C , CM000685.2:g.154993050T>C	GRCh38
NC_000023.10:g.154221325T>C , CM000685.1:g.154221325T>C	GRCh37
NC_000023.9:g.153874519T>C	NCBI36
NG_011403.1:g.34674A>G
NG_011403.2:g.34674A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.487A>G MANE Select	ENSP00000353393.4:p.Asn163Asp
ENST00000647125.1:c.*273A>G	ENSP00000496062.1:n.*273A>G
ENST00000360256.8:c.487A>G	ENSP00000353393.4:p.Asn163Asp
ENST00000423959.5:c.382A>G	ENSP00000409446.1:p.Asn128Asp
ENST00000453950.1:c.469A>G	ENSP00000389153.1:p.Asn157Asp
NM_000132.3:c.487A>G	NP_000123.1:p.Asn163Asp
XM_011531126.1:c.382A>G	XP_011529428.1:p.Asn128Asp
NM_000132.4:c.487A>G MANE Select	NP_000123.1:p.Asn163Asp