Canonical Allele Identifier: CA12522508

Gene: CHRM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.137017188T>A , CM000669.2:g.137017188T>A	GRCh38
NC_000007.13:g.136701935T>A , CM000669.1:g.136701935T>A	GRCh37
NC_000007.12:g.136352475T>A	NCBI36
NG_011846.2:g.153537T>A , LRG_405:g.153537T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680005.1:c.*922T>A MANE Select	ENSP00000505686.1:n.*922T>A
ENST00000445907.6:c.*922T>A	ENSP00000399745.2:n.*922T>A
NR_046103.1:n.341+15606A>T
XM_011515769.1:c.*922T>A	XP_011514071.1:n.*922T>A
XM_011515770.1:c.*922T>A	XP_011514072.1:n.*922T>A
XM_011515771.1:c.*922T>A	XP_011514073.1:n.*922T>A
XM_024446648.1:c.*922T>A	XP_024302416.1:n.*922T>A
NM_001006626.2:c.*922T>A	NP_001006627.1:n.*922T>A
NM_001006627.2:c.*922T>A	NP_001006628.1:n.*922T>A
NM_001006628.2:c.*922T>A	NP_001006629.1:n.*922T>A
NM_001006629.2:c.*922T>A	NP_001006630.1:n.*922T>A
NM_001006631.2:c.*922T>A	NP_001006632.1:n.*922T>A
NM_001006632.2:c.*922T>A	NP_001006633.1:n.*922T>A
NM_000739.3:c.*922T>A	NP_000730.1:n.*922T>A
NM_001006626.3:c.*922T>A	NP_001006627.1:n.*922T>A
NM_001006627.3:c.*922T>A	NP_001006628.1:n.*922T>A
NM_001006628.3:c.*922T>A	NP_001006629.1:n.*922T>A
NM_001006629.3:c.*922T>A	NP_001006630.1:n.*922T>A
NM_001006630.2:c.*922T>A MANE Select	NP_001006631.1:n.*922T>A
NM_001006631.3:c.*922T>A	NP_001006632.1:n.*922T>A
NM_001006632.3:c.*922T>A	NP_001006633.1:n.*922T>A
NM_001378972.1:c.*922T>A	NP_001365901.1:n.*922T>A
NM_001378973.1:c.*922T>A	NP_001365902.1:n.*922T>A