Canonical Allele Identifier: CA393576214

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78911190G>C (hg19) ; chr15:g.78618848G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618848G>C , CM000677.2:g.78618848G>C	GRCh38
NC_000015.9:g.78911190G>C , CM000677.1:g.78911190G>C	GRCh37
NC_000015.8:g.76698245G>C	NCBI36
NG_016143.1:g.7448C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.150C>G MANE Select	ENSP00000315602.5:p.Ile50Met
ENST00000326828.5:c.150C>G	ENSP00000315602.5:p.Ile50Met
ENST00000348639.7:c.150C>G	ENSP00000267951.4:p.Ile50Met
ENST00000559080.1:c.-52C>G	ENSP00000453993.1:n.-52C>G
ENST00000559658.5:c.150C>G	ENSP00000452896.1:p.Ile50Met
ENST00000561128.1:n.145C>G
NM_000743.4:c.150C>G	NP_000734.2:p.Ile50Met
NM_001166694.1:c.150C>G	NP_001160166.1:p.Ile50Met
NR_046313.1:n.651C>G
XM_006720382.1:c.-52C>G	XP_006720445.1:n.-52C>G
XM_011521173.1:c.69C>G	XP_011519475.1:p.Ile23Met
XM_006720382.3:c.-52C>G	XP_006720445.1:n.-52C>G
NM_000743.5:c.150C>G MANE Select	NP_000734.2:p.Ile50Met
NM_001166694.2:c.150C>G	NP_001160166.1:p.Ile50Met
NR_046313.2:n.352C>G