Canonical Allele Identifier: CA1630835156

Gene: CHRNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42697490G= , CM000670.2:g.42697490G=	GRCh38
NC_000008.10:g.42552633G= , CM000670.1:g.42552633G=	GRCh37
NC_000008.9:g.42671790G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000749.5:c.-57G= MANE Select	NP_000740.1:n.-57G=
ENST00000289957.3:c.-57G= MANE Select	ENSP00000289957.2:n.-57G=
NM_000749.3:c.-57G=	NP_000740.1:n.-57G=
NM_000749.4:c.-57G=	NP_000740.1:n.-57G=
NM_001347717.1:c.-412G=	NP_001334646.1:n.-412G=
NM_001347717.2:c.-412G=	NP_001334646.1:n.-412G=
ENST00000289957.2:c.-57G=	ENSP00000289957.2:n.-57G=
ENST00000531610.5:n.115G=
ENST00000534391.1:c.-412G=	ENSP00000433913.1:n.-412G=
XR_001745886.1:n.1622C=
XR_001745887.1:n.552C=
XR_949716.1:n.919C=
XR_949717.1:n.1617C=