Canonical Allele Identifier: CA1745950605

Gene: CHRM2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.136958947C= , CM000669.2:g.136958947C=	GRCh38
NC_000007.13:g.136643694C= , CM000669.1:g.136643694C=	GRCh37
NC_000007.12:g.136294234C=	NCBI36
NG_011846.2:g.95296C= , LRG_405:g.95296C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001006630.2:c.-124-33240C= MANE Select	NP_001006631.1:n.-124-33240C=
ENST00000680005.1:c.-124-33240C= MANE Select	ENSP00000505686.1:n.-124-33240C=
NM_000739.2:c.-124-33240C= , LRG_405t1:c.-124-33240C=	NP_000730.1:n.-124-33240C=
NM_000739.3:c.-124-33240C=	NP_000730.1:n.-124-33240C=
NM_001006626.1:c.-125+7867C=	NP_001006627.1:n.-125+7867C=
NM_001006626.2:c.-125+7867C=	NP_001006627.1:n.-125+7867C=
NM_001006626.3:c.-125+7867C=	NP_001006627.1:n.-125+7867C=
NM_001006627.1:c.-46-55873C=	NP_001006628.1:n.-46-55873C=
NM_001006627.2:c.-46-55873C=	NP_001006628.1:n.-46-55873C=
NM_001006627.3:c.-46-55873C=	NP_001006628.1:n.-46-55873C=
NM_001006628.1:c.-124-33240C=	NP_001006629.1:n.-124-33240C=
NM_001006628.2:c.-124-33240C=	NP_001006629.1:n.-124-33240C=
NM_001006628.3:c.-124-33240C=	NP_001006629.1:n.-124-33240C=
NM_001006629.1:c.-46-55873C=	NP_001006630.1:n.-46-55873C=
NM_001006629.2:c.-46-55873C=	NP_001006630.1:n.-46-55873C=
NM_001006629.3:c.-46-55873C=	NP_001006630.1:n.-46-55873C=
NM_001006630.1:c.-124-33240C= , LRG_405t2:c.-124-33240C=	NP_001006631.1:n.-124-33240C=
NM_001006631.1:c.-124-33240C=	NP_001006632.1:n.-124-33240C=
NM_001006631.2:c.-124-33240C=	NP_001006632.1:n.-124-33240C=
NM_001006631.3:c.-124-33240C=	NP_001006632.1:n.-124-33240C=
NM_001006632.1:c.-46-55873C=	NP_001006633.1:n.-46-55873C=
NM_001006632.2:c.-46-55873C=	NP_001006633.1:n.-46-55873C=
NM_001006632.3:c.-46-55873C=	NP_001006633.1:n.-46-55873C=
NM_001378972.1:c.-236-28044C=	NP_001365901.1:n.-236-28044C=
NM_001378973.1:c.-46-55873C=	NP_001365902.1:n.-46-55873C=
NR_046103.1:n.342-56946G=
ENST00000320658.9:c.-46-55873C=	ENSP00000319984.5:n.-46-55873C=
ENST00000401861.1:c.-125+7867C=	ENSP00000384401.1:n.-125+7867C=
ENST00000445907.6:c.-46-55873C=	ENSP00000399745.2:n.-46-55873C=
ENST00000453373.5:c.-46-55873C=	ENSP00000415386.1:n.-46-55873C=
XM_011515771.1:c.-125+19762C=	XP_011514073.1:n.-125+19762C=
XM_024446648.1:c.-236-28044C=	XP_024302416.1:n.-236-28044C=