Canonical Allele Identifier: CA851922301

Gene: CHRNB3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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