Canonical Allele Identifier: CA369485767

Gene: CHRM2

Linked Data

• ClinVar Variation Id: 1988032
• ClinVar RCV Id: RCV002781094
• gnomAD v4: 7-137014981-T-A
• MyVariant Identifiers: chr7:g.136699728T>A (hg19) ; chr7:g.137014981T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.137014981T>A , CM000669.2:g.137014981T>A	GRCh38
NC_000007.13:g.136699728T>A , CM000669.1:g.136699728T>A	GRCh37
NC_000007.12:g.136350268T>A	NCBI36
NG_011846.2:g.151330T>A , LRG_405:g.151330T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680005.1:c.116T>A MANE Select	ENSP00000505686.1:p.Ile39Asn
ENST00000320658.9:c.116T>A	ENSP00000319984.5:p.Ile39Asn
ENST00000401861.1:c.116T>A	ENSP00000384401.1:p.Ile39Asn
ENST00000445907.6:c.116T>A	ENSP00000399745.2:p.Ile39Asn
ENST00000453373.5:c.116T>A	ENSP00000415386.1:p.Ile39Asn
NM_000739.2:c.116T>A , LRG_405t1:c.116T>A	NP_000730.1:p.Ile39Asn
NM_001006626.1:c.116T>A	NP_001006627.1:p.Ile39Asn
NM_001006627.1:c.116T>A	NP_001006628.1:p.Ile39Asn
NM_001006628.1:c.116T>A	NP_001006629.1:p.Ile39Asn
NM_001006629.1:c.116T>A	NP_001006630.1:p.Ile39Asn
NM_001006630.1:c.116T>A , LRG_405t2:c.116T>A	NP_001006631.1:p.Ile39Asn
NM_001006631.1:c.116T>A	NP_001006632.1:p.Ile39Asn
NM_001006632.1:c.116T>A	NP_001006633.1:p.Ile39Asn
NR_046103.1:n.341+17813A>T
XM_011515769.1:c.116T>A	XP_011514071.1:p.Ile39Asn
XM_011515770.1:c.116T>A	XP_011514072.1:p.Ile39Asn
XM_011515771.1:c.116T>A	XP_011514073.1:p.Ile39Asn
XM_024446648.1:c.116T>A	XP_024302416.1:p.Ile39Asn
NM_001006626.2:c.116T>A	NP_001006627.1:p.Ile39Asn
NM_001006627.2:c.116T>A	NP_001006628.1:p.Ile39Asn
NM_001006628.2:c.116T>A	NP_001006629.1:p.Ile39Asn
NM_001006629.2:c.116T>A	NP_001006630.1:p.Ile39Asn
NM_001006631.2:c.116T>A	NP_001006632.1:p.Ile39Asn
NM_001006632.2:c.116T>A	NP_001006633.1:p.Ile39Asn
NM_000739.3:c.116T>A	NP_000730.1:p.Ile39Asn
NM_001006626.3:c.116T>A	NP_001006627.1:p.Ile39Asn
NM_001006627.3:c.116T>A	NP_001006628.1:p.Ile39Asn
NM_001006628.3:c.116T>A	NP_001006629.1:p.Ile39Asn
NM_001006629.3:c.116T>A	NP_001006630.1:p.Ile39Asn
NM_001006630.2:c.116T>A MANE Select	NP_001006631.1:p.Ile39Asn
NM_001006631.3:c.116T>A	NP_001006632.1:p.Ile39Asn
NM_001006632.3:c.116T>A	NP_001006633.1:p.Ile39Asn
NM_001378972.1:c.116T>A	NP_001365901.1:p.Ile39Asn
NM_001378973.1:c.116T>A	NP_001365902.1:p.Ile39Asn