Canonical Allele Identifier: CA414920707

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154250809T>G (hg19) ; chrX:g.155022534T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022534T>G , CM000685.2:g.155022534T>G	GRCh38
NC_000023.10:g.154250809T>G , CM000685.1:g.154250809T>G	GRCh37
NC_000023.9:g.153904003T>G	NCBI36
NG_011403.1:g.5190A>C
NG_011403.2:g.5190A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.19A>C MANE Select	ENSP00000353393.4:p.Thr7Pro
ENST00000647125.1:c.19A>C	ENSP00000496062.1:p.Thr7Pro
ENST00000360256.8:c.19A>C	ENSP00000353393.4:p.Thr7Pro
ENST00000423959.5:c.38+4246A>C	ENSP00000409446.1:n.38+4246A>C
ENST00000453950.1:c.39-38A>C	ENSP00000389153.1:n.39-38A>C
NM_000132.3:c.19A>C	NP_000123.1:p.Thr7Pro
XM_011531126.1:c.38+4246A>C	XP_011529428.1:n.38+4246A>C
NM_000132.4:c.19A>C MANE Select	NP_000123.1:p.Thr7Pro