Canonical Allele Identifier: CA414920109

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225359G>C (hg19) ; chrX:g.154997084G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997084G>C , CM000685.2:g.154997084G>C	GRCh38
NC_000023.10:g.154225359G>C , CM000685.1:g.154225359G>C	GRCh37
NC_000023.9:g.153878553G>C	NCBI36
NG_011403.1:g.30640C>G
NG_011403.2:g.30640C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.277C>G MANE Select	ENSP00000353393.4:p.Pro93Ala
ENST00000647125.1:c.*63C>G	ENSP00000496062.1:n.*63C>G
ENST00000360256.8:c.277C>G	ENSP00000353393.4:p.Pro93Ala
ENST00000423959.5:c.172C>G	ENSP00000409446.1:p.Pro58Ala
ENST00000453950.1:c.259C>G	ENSP00000389153.1:p.Pro87Ala
NM_000132.3:c.277C>G	NP_000123.1:p.Pro93Ala
XM_011531126.1:c.172C>G	XP_011529428.1:p.Pro58Ala
NM_000132.4:c.277C>G MANE Select	NP_000123.1:p.Pro93Ala