Canonical Allele Identifier: CA273876474
Gene: CHRNA5 HGNC NCBI

Linked Data

dbSNP Id: rs929018427
gnomAD v4: 15-78565546-T-A
MyVariant Identifiers: chr15:g.78565546T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78565546T>A , CM000677.2:g.78565546T>A GRCh38
NC_000015.9:g.78857888T>A , CM000677.1:g.78857888T>A GRCh37
NC_000015.8:g.76644943T>A NCBI36
NG_023328.1:g.5027T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299565.9:c.-174T>A MANE Select ENSP00000299565.5:n.-174T>A
NM_000745.3:c.-174T>A NP_000736.2:n.-174T>A
NM_001307945.1:c.-174T>A NP_001294874.1:n.-174T>A
XM_005254142.2:c.-174T>A XP_005254199.1:n.-174T>A
NM_001307945.2:c.-174T>A NP_001294874.1:n.-174T>A
NM_000745.4:c.-174T>A MANE Select NP_000736.2:n.-174T>A
NM_001395171.1:c.-174T>A NP_001382100.1:n.-174T>A
NM_001395172.1:c.-174T>A NP_001382101.1:n.-174T>A
NM_001395173.1:c.-174T>A NP_001382102.1:n.-174T>A
NM_001395174.1:c.-174T>A NP_001382103.1:n.-174T>A
NM_001395175.1:c.-174T>A NP_001382104.1:n.-174T>A
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