Canonical Allele Identifier: CA414907552

Gene: F8

Linked Data

• dbSNP Id: rs782217392
• MyVariant Identifiers: chrX:g.154091435C>G (hg19) ; chrX:g.154863160C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863160C>G , CM000685.2:g.154863160C>G	GRCh38
NC_000023.10:g.154091435C>G , CM000685.1:g.154091435C>G	GRCh37
NC_000023.9:g.153744629C>G	NCBI36
NG_011403.1:g.164564G>C
NG_011403.2:g.164564G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6497G>C MANE Select	ENSP00000353393.4:p.Arg2166Pro
ENST00000644698.1:c.230G>C	ENSP00000495706.1:p.Arg77Pro
ENST00000330287.10:c.92G>C	ENSP00000327895.6:p.Arg31Pro
ENST00000360256.8:c.6497G>C	ENSP00000353393.4:p.Arg2166Pro
NM_000132.3:c.6497G>C	NP_000123.1:p.Arg2166Pro
NM_019863.2:c.92G>C	NP_063916.1:p.Arg31Pro
XM_011531126.1:c.6392G>C	XP_011529428.1:p.Arg2131Pro
NM_000132.4:c.6497G>C MANE Select	NP_000123.1:p.Arg2166Pro
NM_019863.3:c.92G>C	NP_063916.1:p.Arg31Pro