Canonical Allele Identifier: CA393586606

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1457167215
• gnomAD v3: 15-78602226-G-C
• gnomAD v4: 15-78602226-G-C
• MyVariant Identifiers: chr15:g.78894568G>C (hg19) ; chr15:g.78602226G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602226G>C , CM000677.2:g.78602226G>C	GRCh38
NC_000015.9:g.78894568G>C , CM000677.1:g.78894568G>C	GRCh37
NC_000015.8:g.76681623G>C	NCBI36
NG_016143.1:g.24070C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.416C>G MANE Select	ENSP00000315602.5:p.Ala139Gly
ENST00000326828.5:c.416C>G	ENSP00000315602.5:p.Ala139Gly
ENST00000348639.7:c.416C>G	ENSP00000267951.4:p.Ala139Gly
ENST00000558903.1:n.123C>G
ENST00000559658.5:c.416C>G	ENSP00000452896.1:p.Ala139Gly
NM_000743.4:c.416C>G	NP_000734.2:p.Ala139Gly
NM_001166694.1:c.416C>G	NP_001160166.1:p.Ala139Gly
NR_046313.1:n.917C>G
XM_006720382.1:c.215C>G	XP_006720445.1:p.Ala72Gly
XM_011521173.1:c.335C>G	XP_011519475.1:p.Ala112Gly
XM_006720382.3:c.215C>G	XP_006720445.1:p.Ala72Gly
NM_000743.5:c.416C>G MANE Select	NP_000734.2:p.Ala139Gly
NM_001166694.2:c.416C>G	NP_001160166.1:p.Ala139Gly
NR_046313.2:n.618C>G