Canonical Allele Identifier: CA1107634874
Gene: CHRM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.137008992T>C , CM000669.2:g.137008992T>C GRCh38
NC_000007.13:g.136693739T>C , CM000669.1:g.136693739T>C GRCh37
NC_000007.12:g.136344279T>C NCBI36
NG_011846.2:g.145341T>C , LRG_405:g.145341T>C

Transcript Alleles

HGVS Amino-acid change
NM_000739.2:c.-46-5828T>C , LRG_405t1:c.-46-5828T>C NP_000730.1:p.=
NM_001006626.1:c.-46-5828T>C NP_001006627.1:p.=
NM_001006627.1:c.-46-5828T>C NP_001006628.1:p.=
NM_001006628.1:c.-46-5828T>C NP_001006629.1:p.=
NM_001006629.1:c.-46-5828T>C NP_001006630.1:p.=
NM_001006630.1:c.-46-5828T>C , LRG_405t2:c.-46-5828T>C NP_001006631.1:p.=
NM_001006631.1:c.-46-5828T>C NP_001006632.1:p.=
NM_001006632.1:c.-46-5828T>C NP_001006633.1:p.=
NR_046103.1:n.341+23802A>G
XM_011515769.1:c.-46-5828T>C XP_011514071.1:p.=
XM_011515770.1:c.-46-5828T>C XP_011514072.1:p.=
XM_011515771.1:c.-46-5828T>C XP_011514073.1:p.=
XM_024446648.1:c.-46-5828T>C XP_024302416.1:p.=
NM_001006626.2:c.-46-5828T>C NP_001006627.1:p.=
NM_001006627.2:c.-46-5828T>C NP_001006628.1:p.=
NM_001006628.2:c.-46-5828T>C NP_001006629.1:p.=
NM_001006629.2:c.-46-5828T>C NP_001006630.1:p.=
NM_001006631.2:c.-46-5828T>C NP_001006632.1:p.=
NM_001006632.2:c.-46-5828T>C NP_001006633.1:p.=
NM_000739.3:c.-46-5828T>C NP_000730.1:p.=
NM_001006626.3:c.-46-5828T>C NP_001006627.1:p.=
NM_001006627.3:c.-46-5828T>C NP_001006628.1:p.=
NM_001006628.3:c.-46-5828T>C NP_001006629.1:p.=
NM_001006629.3:c.-46-5828T>C NP_001006630.1:p.=
NM_001006630.2:c.-46-5828T>C NP_001006631.1:p.=
NM_001006631.3:c.-46-5828T>C NP_001006632.1:p.=
NM_001006632.3:c.-46-5828T>C NP_001006633.1:p.=
NM_001378972.1:c.-46-5828T>C NP_001365901.1:p.=
NM_001378973.1:c.-46-5828T>C NP_001365902.1:p.=
ENST00000320658.9:c.-46-5828T>C ENSP00000319984.5:p.=
ENST00000401861.1:c.-46-5828T>C ENSP00000384401.1:p.=
ENST00000445907.6:c.-46-5828T>C ENSP00000399745.2:p.=
ENST00000453373.5:c.-46-5828T>C ENSP00000415386.1:p.=