Canonical Allele Identifier: CA414920049

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225332T>C (hg19) ; chrX:g.154997057T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997057T>C , CM000685.2:g.154997057T>C	GRCh38
NC_000023.10:g.154225332T>C , CM000685.1:g.154225332T>C	GRCh37
NC_000023.9:g.153878526T>C	NCBI36
NG_011403.1:g.30667A>G
NG_011403.2:g.30667A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.304A>G MANE Select	ENSP00000353393.4:p.Thr102Ala
ENST00000647125.1:c.*90A>G	ENSP00000496062.1:n.*90A>G
ENST00000360256.8:c.304A>G	ENSP00000353393.4:p.Thr102Ala
ENST00000423959.5:c.199A>G	ENSP00000409446.1:p.Thr67Ala
ENST00000453950.1:c.286A>G	ENSP00000389153.1:p.Thr96Ala
NM_000132.3:c.304A>G	NP_000123.1:p.Thr102Ala
XM_011531126.1:c.199A>G	XP_011529428.1:p.Thr67Ala
NM_000132.4:c.304A>G MANE Select	NP_000123.1:p.Thr102Ala