Canonical Allele Identifier: CA519384149

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225330T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997055T>G , CM000685.2:g.154997055T>G	GRCh38
NC_000023.10:g.154225330T>G , CM000685.1:g.154225330T>G	GRCh37
NC_000023.9:g.153878524T>G	NCBI36
NG_011403.1:g.30669A>C
NG_011403.2:g.30669A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.306A>C MANE Select	ENSP00000353393.4:p.Thr102=
ENST00000647125.1:c.*92A>C	ENSP00000496062.1:n.*92A>C
ENST00000360256.8:c.306A>C	ENSP00000353393.4:p.Thr102=
ENST00000423959.5:c.201A>C	ENSP00000409446.1:p.Thr67=
ENST00000453950.1:c.288A>C	ENSP00000389153.1:p.Thr96=
NM_000132.3:c.306A>C	NP_000123.1:p.Thr102=
XM_011531126.1:c.201A>C	XP_011529428.1:p.Thr67=
NM_000132.4:c.306A>C MANE Select	NP_000123.1:p.Thr102=