Canonical Allele Identifier: CA2629789041

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78616939-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78616939A>G , CM000677.2:g.78616939A>G	GRCh38
NC_000015.9:g.78909281A>G , CM000677.1:g.78909281A>G	GRCh37
NC_000015.8:g.76696336A>G	NCBI36
NG_016143.1:g.9357T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+85T>C MANE Select	ENSP00000315602.5:n.377+85T>C
ENST00000326828.5:c.377+85T>C	ENSP00000315602.5:n.377+85T>C
ENST00000348639.7:c.377+85T>C	ENSP00000267951.4:n.377+85T>C
ENST00000559658.5:c.377+85T>C	ENSP00000452896.1:n.377+85T>C
NM_000743.4:c.377+85T>C	NP_000734.2:n.377+85T>C
NM_001166694.1:c.377+85T>C	NP_001160166.1:n.377+85T>C
NR_046313.1:n.878+85T>C
XM_006720382.1:c.176+85T>C	XP_006720445.1:n.176+85T>C
XM_011521173.1:c.296+85T>C	XP_011519475.1:n.296+85T>C
XM_006720382.3:c.176+85T>C	XP_006720445.1:n.176+85T>C
NM_000743.5:c.377+85T>C MANE Select	NP_000734.2:n.377+85T>C
NM_001166694.2:c.377+85T>C	NP_001160166.1:n.377+85T>C
NR_046313.2:n.579+85T>C