Canonical Allele Identifier: CA414902325

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154159746C>G (hg19) ; chrX:g.154931471C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154931471C>G , CM000685.2:g.154931471C>G	GRCh38
NC_000023.10:g.154159746C>G , CM000685.1:g.154159746C>G	GRCh37
NC_000023.9:g.153812940C>G	NCBI36
NG_011403.1:g.96253G>C
NG_011403.2:g.96253G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.2319G>C MANE Select	ENSP00000353393.4:p.Lys773Asn
ENST00000647125.1:c.*1985G>C	ENSP00000496062.1:n.*1985G>C
ENST00000360256.8:c.2319G>C	ENSP00000353393.4:p.Lys773Asn
NM_000132.3:c.2319G>C	NP_000123.1:p.Lys773Asn
XM_011531126.1:c.2214G>C	XP_011529428.1:p.Lys738Asn
NM_000132.4:c.2319G>C MANE Select	NP_000123.1:p.Lys773Asn