Canonical Allele Identifier: CA1107664325
Gene: CHRM2 HGNC NCBI

Linked Data

dbSNP Id: rs1800102562

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.136946884C>T , CM000669.2:g.136946884C>T GRCh38
NC_000007.13:g.136631631C>T , CM000669.1:g.136631631C>T GRCh37
NC_000007.12:g.136282171C>T NCBI36
NG_011846.2:g.83233C>T , LRG_405:g.83233C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000680005.1:c.-124-45303C>T MANE Select ENSP00000505686.1:n.-124-45303C>T
ENST00000320658.9:c.-46-67936C>T ENSP00000319984.5:n.-46-67936C>T
ENST00000401861.1:c.-202-4119C>T ENSP00000384401.1:n.-202-4119C>T
ENST00000445907.6:c.-46-67936C>T ENSP00000399745.2:n.-46-67936C>T
ENST00000453373.5:c.-46-67936C>T ENSP00000415386.1:n.-46-67936C>T
NM_000739.2:c.-124-45303C>T , LRG_405t1:c.-124-45303C>T NP_000730.1:n.-124-45303C>T
NM_001006626.1:c.-202-4119C>T NP_001006627.1:n.-202-4119C>T
NM_001006627.1:c.-46-67936C>T NP_001006628.1:n.-46-67936C>T
NM_001006628.1:c.-124-45303C>T NP_001006629.1:n.-124-45303C>T
NM_001006629.1:c.-46-67936C>T NP_001006630.1:n.-46-67936C>T
NM_001006630.1:c.-124-45303C>T , LRG_405t2:c.-124-45303C>T NP_001006631.1:n.-124-45303C>T
NM_001006631.1:c.-124-45303C>T NP_001006632.1:n.-124-45303C>T
NM_001006632.1:c.-46-67936C>T NP_001006633.1:n.-46-67936C>T
NR_046103.1:n.342-44883G>A
XM_011515771.1:c.-125+7699C>T XP_011514073.1:n.-125+7699C>T
XM_024446648.1:c.-236-40107C>T XP_024302416.1:n.-236-40107C>T
NM_001006626.2:c.-202-4119C>T NP_001006627.1:n.-202-4119C>T
NM_001006627.2:c.-46-67936C>T NP_001006628.1:n.-46-67936C>T
NM_001006628.2:c.-124-45303C>T NP_001006629.1:n.-124-45303C>T
NM_001006629.2:c.-46-67936C>T NP_001006630.1:n.-46-67936C>T
NM_001006631.2:c.-124-45303C>T NP_001006632.1:n.-124-45303C>T
NM_001006632.2:c.-46-67936C>T NP_001006633.1:n.-46-67936C>T
NM_000739.3:c.-124-45303C>T NP_000730.1:n.-124-45303C>T
NM_001006626.3:c.-202-4119C>T NP_001006627.1:n.-202-4119C>T
NM_001006627.3:c.-46-67936C>T NP_001006628.1:n.-46-67936C>T
NM_001006628.3:c.-124-45303C>T NP_001006629.1:n.-124-45303C>T
NM_001006629.3:c.-46-67936C>T NP_001006630.1:n.-46-67936C>T
NM_001006630.2:c.-124-45303C>T MANE Select NP_001006631.1:n.-124-45303C>T
NM_001006631.3:c.-124-45303C>T NP_001006632.1:n.-124-45303C>T
NM_001006632.3:c.-46-67936C>T NP_001006633.1:n.-46-67936C>T
NM_001378972.1:c.-236-40107C>T NP_001365901.1:n.-236-40107C>T
NM_001378973.1:c.-46-67936C>T NP_001365902.1:n.-46-67936C>T