Canonical Allele Identifier: CA414919769

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154221392C>G (hg19) ; chrX:g.154993117C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993117C>G , CM000685.2:g.154993117C>G	GRCh38
NC_000023.10:g.154221392C>G , CM000685.1:g.154221392C>G	GRCh37
NC_000023.9:g.153874586C>G	NCBI36
NG_011403.1:g.34607G>C
NG_011403.2:g.34607G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.420G>C MANE Select	ENSP00000353393.4:p.Arg140Ser
ENST00000647125.1:c.*206G>C	ENSP00000496062.1:n.*206G>C
ENST00000360256.8:c.420G>C	ENSP00000353393.4:p.Arg140Ser
ENST00000423959.5:c.315G>C	ENSP00000409446.1:p.Arg105Ser
ENST00000453950.1:c.402G>C	ENSP00000389153.1:p.Arg134Ser
NM_000132.3:c.420G>C	NP_000123.1:p.Arg140Ser
XM_011531126.1:c.315G>C	XP_011529428.1:p.Arg105Ser
NM_000132.4:c.420G>C MANE Select	NP_000123.1:p.Arg140Ser