Canonical Allele Identifier: CA733506051

Gene: CHRM3

Linked Data

• dbSNP Id: rs2355230
• gnomAD v3: 1-239621865-C-T
• gnomAD v4: 1-239621865-C-T
• MyVariant Identifiers: chr1:g.239785165C>T (hg19) ; chr1:g.239621865C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.239621865C>T , CM000663.2:g.239621865C>T	GRCh38
NC_000001.10:g.239785165C>T , CM000663.1:g.239785165C>T	GRCh37
NC_000001.9:g.237851788C>T	NCBI36
NG_032046.2:g.239936C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615928.5:c.-312-10359C>T	ENSP00000482377.1:n.-312-10359C>T
ENST00000675184.1:c.-312-10359C>T	ENSP00000502349.1:n.-312-10359C>T
ENST00000676153.1:c.-312-10359C>T MANE Select	ENSP00000502667.1:n.-312-10359C>T
ENST00000676433.1:c.-313+8247C>T	ENSP00000502013.1:n.-313+8247C>T
ENST00000468573.5:n.872-10359C>T
XM_005273032.2:c.-312-10359C>T	XP_005273089.1:n.-312-10359C>T
XM_011544041.1:c.-312-10359C>T	XP_011542343.1:n.-312-10359C>T
XM_011544042.1:c.-801-10359C>T	XP_011542344.1:n.-801-10359C>T
XM_011544043.1:c.-645-10359C>T	XP_011542345.1:n.-645-10359C>T
XM_011544044.1:c.-416-10359C>T	XP_011542346.1:n.-416-10359C>T
XM_011544045.1:c.-541-10359C>T	XP_011542347.1:n.-541-10359C>T
XM_011544046.1:c.-249-56321C>T	XP_011542348.1:n.-249-56321C>T
XM_011544047.1:c.-185-10359C>T	XP_011542349.1:n.-185-10359C>T
XR_949316.1:n.332+9506G>A
XR_949317.1:n.332+9506G>A
XR_949318.1:n.332+9506G>A
NM_001347716.1:c.-541-10359C>T	NP_001334645.1:n.-541-10359C>T
XM_005273032.3:c.-312-10359C>T	XP_005273089.1:n.-312-10359C>T
XM_011544041.2:c.-312-10359C>T	XP_011542343.1:n.-312-10359C>T
XM_011544043.2:c.-645-10359C>T	XP_011542345.1:n.-645-10359C>T
XM_011544044.2:c.-416-10359C>T	XP_011542346.1:n.-416-10359C>T
XM_011544046.2:c.-249-56321C>T	XP_011542348.1:n.-249-56321C>T
XM_011544047.2:c.-185-10359C>T	XP_011542349.1:n.-185-10359C>T
XM_017000152.2:c.-312-10359C>T	XP_016855641.1:n.-312-10359C>T
XM_017000153.1:c.-312-10359C>T	XP_016855642.1:n.-312-10359C>T
XM_017000154.1:c.-312-10359C>T	XP_016855643.1:n.-312-10359C>T
XM_017000155.1:c.-353-56321C>T	XP_016855644.1:n.-353-56321C>T
XM_017000156.1:c.-416-10359C>T	XP_016855645.1:n.-416-10359C>T
XM_017000157.2:c.-312-10359C>T	XP_016855646.1:n.-312-10359C>T
XM_017000158.1:c.-249-56321C>T	XP_016855647.1:n.-249-56321C>T
XM_017000159.1:c.-122-56321C>T	XP_016855648.1:n.-122-56321C>T
XM_017000161.1:c.-353-56321C>T	XP_016855650.1:n.-353-56321C>T
XM_017000162.1:c.-185-10359C>T	XP_016855651.1:n.-185-10359C>T
XR_001738554.1:n.843+9506G>A
XR_001738555.1:n.412+9506G>A
XR_001738556.1:n.1499+9506G>A
XR_001738557.1:n.843+9506G>A
XR_001738558.1:n.843+9506G>A
NM_001347716.2:c.-541-10359C>T	NP_001334645.1:n.-541-10359C>T
NM_001375978.1:c.-312-10359C>T MANE Select	NP_001362907.1:n.-312-10359C>T
NM_001375979.1:c.-249-56321C>T	NP_001362908.1:n.-249-56321C>T
NM_001375980.1:c.-249-56321C>T	NP_001362909.1:n.-249-56321C>T
NM_001375981.1:c.-312-10359C>T	NP_001362910.1:n.-312-10359C>T
NM_001375982.1:c.-312-10359C>T	NP_001362911.1:n.-312-10359C>T
NM_001375983.1:c.-353-56321C>T	NP_001362912.1:n.-353-56321C>T
NM_001375984.1:c.-416-10359C>T	NP_001362913.1:n.-416-10359C>T
NM_001375985.1:c.-353-56321C>T	NP_001362914.1:n.-353-56321C>T
NR_164748.1:n.869-10359C>T