Canonical Allele Identifier: CA13851057

Gene: TM9SF2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.99544698G>A , CM000675.2:g.99544698G>A	GRCh38
NC_000013.10:g.100196952G>A , CM000675.1:g.100196952G>A	GRCh37
NC_000013.9:g.98994953G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376387.5:c.1150+703G>A MANE Select	ENSP00000365567.3:n.1150+703G>A
ENST00000642475.1:c.1150+703G>A	ENSP00000493515.1:n.1150+703G>A
ENST00000376387.4:c.1150+703G>A	ENSP00000365567.3:n.1150+703G>A
NM_004800.2:c.1150+703G>A	NP_004791.1:n.1150+703G>A
NM_004800.3:c.1150+703G>A MANE Select	NP_004791.1:n.1150+703G>A