Canonical Allele Identifier: CA491626331

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1433035046
• gnomAD v2: 15-78909410-G-A
• gnomAD v4: 15-78617068-G-A
• MyVariant Identifiers: chr15:g.78909410G>A (hg19) ; chr15:g.78617068G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617068G>A , CM000677.2:g.78617068G>A	GRCh38
NC_000015.9:g.78909410G>A , CM000677.1:g.78909410G>A	GRCh37
NC_000015.8:g.76696465G>A	NCBI36
NG_016143.1:g.9228C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.333C>T MANE Select	ENSP00000315602.5:p.Val111=
ENST00000326828.5:c.333C>T	ENSP00000315602.5:p.Val111=
ENST00000348639.7:c.333C>T	ENSP00000267951.4:p.Val111=
ENST00000559658.5:c.333C>T	ENSP00000452896.1:p.Val111=
NM_000743.4:c.333C>T	NP_000734.2:p.Val111=
NM_001166694.1:c.333C>T	NP_001160166.1:p.Val111=
NR_046313.1:n.834C>T
XM_006720382.1:c.132C>T	XP_006720445.1:p.Val44=
XM_011521173.1:c.252C>T	XP_011519475.1:p.Val84=
XM_006720382.3:c.132C>T	XP_006720445.1:p.Val44=
NM_000743.5:c.333C>T MANE Select	NP_000734.2:p.Val111=
NM_001166694.2:c.333C>T	NP_001160166.1:p.Val111=
NR_046313.2:n.535C>T