Canonical Allele Identifier: CA273876534

Gene: CHRNA5

Linked Data

• dbSNP Id: rs1020229973
• gnomAD v4: 15-78565567-C-T
• MyVariant Identifiers: chr15:g.78857909C>T (hg19) ; chr15:g.78565567C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78565567C>T , CM000677.2:g.78565567C>T	GRCh38
NC_000015.9:g.78857909C>T , CM000677.1:g.78857909C>T	GRCh37
NC_000015.8:g.76644964C>T	NCBI36
NG_023328.1:g.5048C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.-153C>T MANE Select	ENSP00000299565.5:n.-153C>T
NM_000745.3:c.-153C>T	NP_000736.2:n.-153C>T
NM_001307945.1:c.-153C>T	NP_001294874.1:n.-153C>T
XM_005254142.2:c.-153C>T	XP_005254199.1:n.-153C>T
NM_001307945.2:c.-153C>T	NP_001294874.1:n.-153C>T
NM_000745.4:c.-153C>T MANE Select	NP_000736.2:n.-153C>T
NM_001395171.1:c.-153C>T	NP_001382100.1:n.-153C>T
NM_001395172.1:c.-153C>T	NP_001382101.1:n.-153C>T
NM_001395173.1:c.-153C>T	NP_001382102.1:n.-153C>T
NM_001395174.1:c.-153C>T	NP_001382103.1:n.-153C>T
NM_001395175.1:c.-153C>T	NP_001382104.1:n.-153C>T