Canonical Allele Identifier: CA1024231014
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929099275
gnomAD v3: 22-20889438-A-T
gnomAD v4: 22-20889438-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20889438A>T , CM000684.2:g.20889438A>T GRCh38
NC_000022.10:g.21243726A>T , CM000684.1:g.21243726A>T GRCh37
NC_000022.9:g.19573726A>T NCBI36
NG_012152.1:g.35435A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*1602A>T MANE Select ENSP00000215730.6:n.*1602A>T
ENST00000215730.11:c.*1602A>T ENSP00000215730.6:n.*1602A>T
NM_004782.3:c.*1602A>T NP_004773.1:n.*1602A>T
NM_004782.4:c.*1602A>T MANE Select NP_004773.1:n.*1602A>T
Search 100 bp 5'
Search 100 bp 3'