Canonical Allele Identifier: CA393584809

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78601872-A-G
• MyVariant Identifiers: chr15:g.78894214A>G (hg19) ; chr15:g.78601872A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601872A>G , CM000677.2:g.78601872A>G	GRCh38
NC_000015.9:g.78894214A>G , CM000677.1:g.78894214A>G	GRCh37
NC_000015.8:g.76681269A>G	NCBI36
NG_016143.1:g.24424T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.770T>C MANE Select	ENSP00000315602.5:p.Phe257Ser
ENST00000326828.5:c.770T>C	ENSP00000315602.5:p.Phe257Ser
ENST00000348639.7:c.770T>C	ENSP00000267951.4:p.Phe257Ser
ENST00000558903.1:n.477T>C
ENST00000559658.5:c.770T>C	ENSP00000452896.1:p.Phe257Ser
NM_000743.4:c.770T>C	NP_000734.2:p.Phe257Ser
NM_001166694.1:c.770T>C	NP_001160166.1:p.Phe257Ser
NR_046313.1:n.1271T>C
XM_006720382.1:c.569T>C	XP_006720445.1:p.Phe190Ser
XM_011521173.1:c.689T>C	XP_011519475.1:p.Phe230Ser
XM_006720382.3:c.569T>C	XP_006720445.1:p.Phe190Ser
NM_000743.5:c.770T>C MANE Select	NP_000734.2:p.Phe257Ser
NM_001166694.2:c.770T>C	NP_001160166.1:p.Phe257Ser
NR_046313.2:n.972T>C