Canonical Allele Identifier: CA167687446

Gene: CHRM2

Linked Data

• dbSNP Id: rs901402844
• gnomAD v3: 7-136911735-T-C
• gnomAD v4: 7-136911735-T-C
• MyVariant Identifiers: chr7:g.136596482T>C (hg19) ; chr7:g.136911735T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.136911735T>C , CM000669.2:g.136911735T>C	GRCh38
NC_000007.13:g.136596482T>C , CM000669.1:g.136596482T>C	GRCh37
NC_000007.12:g.136247022T>C	NCBI36
NG_011846.2:g.48084T>C , LRG_405:g.48084T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680005.1:c.-125+42317T>C MANE Select	ENSP00000505686.1:n.-125+42317T>C
ENST00000320658.9:c.-47+42317T>C	ENSP00000319984.5:n.-47+42317T>C
ENST00000401861.1:c.-202-39268T>C	ENSP00000384401.1:n.-202-39268T>C
ENST00000445907.6:c.-47+42317T>C	ENSP00000399745.2:n.-47+42317T>C
ENST00000453373.5:c.-47+42317T>C	ENSP00000415386.1:n.-47+42317T>C
NM_000739.2:c.-125+42317T>C , LRG_405t1:c.-125+42317T>C	NP_000730.1:n.-125+42317T>C
NM_001006626.1:c.-202-39268T>C	NP_001006627.1:n.-202-39268T>C
NM_001006627.1:c.-47+42317T>C	NP_001006628.1:n.-47+42317T>C
NM_001006628.1:c.-125+42317T>C	NP_001006629.1:n.-125+42317T>C
NM_001006629.1:c.-47+42317T>C	NP_001006630.1:n.-47+42317T>C
NM_001006630.1:c.-125+42317T>C , LRG_405t2:c.-125+42317T>C	NP_001006631.1:n.-125+42317T>C
NM_001006631.1:c.-125+42317T>C	NP_001006632.1:n.-125+42317T>C
NM_001006632.1:c.-47+42317T>C	NP_001006633.1:n.-47+42317T>C
NR_046103.1:n.342-9734A>G
XM_024446648.1:c.-237+42317T>C	XP_024302416.1:n.-237+42317T>C
NM_001006626.2:c.-202-39268T>C	NP_001006627.1:n.-202-39268T>C
NM_001006627.2:c.-47+42317T>C	NP_001006628.1:n.-47+42317T>C
NM_001006628.2:c.-125+42317T>C	NP_001006629.1:n.-125+42317T>C
NM_001006629.2:c.-47+42317T>C	NP_001006630.1:n.-47+42317T>C
NM_001006631.2:c.-125+42317T>C	NP_001006632.1:n.-125+42317T>C
NM_001006632.2:c.-47+42317T>C	NP_001006633.1:n.-47+42317T>C
NM_000739.3:c.-125+42317T>C	NP_000730.1:n.-125+42317T>C
NM_001006626.3:c.-202-39268T>C	NP_001006627.1:n.-202-39268T>C
NM_001006627.3:c.-47+42317T>C	NP_001006628.1:n.-47+42317T>C
NM_001006628.3:c.-125+42317T>C	NP_001006629.1:n.-125+42317T>C
NM_001006629.3:c.-47+42317T>C	NP_001006630.1:n.-47+42317T>C
NM_001006630.2:c.-125+42317T>C MANE Select	NP_001006631.1:n.-125+42317T>C
NM_001006631.3:c.-125+42317T>C	NP_001006632.1:n.-125+42317T>C
NM_001006632.3:c.-47+42317T>C	NP_001006633.1:n.-47+42317T>C
NM_001378972.1:c.-237+42317T>C	NP_001365901.1:n.-237+42317T>C
NM_001378973.1:c.-47+42317T>C	NP_001365902.1:n.-47+42317T>C