Canonical Allele Identifier: CA414910784

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154182236G>T (hg19) ; chrX:g.154953961G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953961G>T , CM000685.2:g.154953961G>T	GRCh38
NC_000023.10:g.154182236G>T , CM000685.1:g.154182236G>T	GRCh37
NC_000023.9:g.153835430G>T	NCBI36
NG_011403.1:g.73763C>A
NG_011403.2:g.73763C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1834C>A MANE Select	ENSP00000353393.4:p.Arg612Ser
ENST00000647125.1:c.*1710C>A	ENSP00000496062.1:n.*1710C>A
ENST00000360256.8:c.1834C>A	ENSP00000353393.4:p.Arg612Ser
NM_000132.3:c.1834C>A	NP_000123.1:p.Arg612Ser
XM_011531126.1:c.1729C>A	XP_011529428.1:p.Arg577Ser
NM_000132.4:c.1834C>A MANE Select	NP_000123.1:p.Arg612Ser