Canonical Allele Identifier: CA1024230655
Gene: SNAP29 HGNC NCBI

Linked Data

ClinVar Variation Id: 901848
ClinVar RCV Id: RCV001147974
dbSNP Id: rs1929072766
gnomAD v3: 22-20888343-A-C
gnomAD v4: 22-20888343-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888343A>C , CM000684.2:g.20888343A>C GRCh38
NC_000022.10:g.21242631A>C , CM000684.1:g.21242631A>C GRCh37
NC_000022.9:g.19572631A>C NCBI36
NG_012152.1:g.34340A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*507A>C MANE Select ENSP00000215730.6:n.*507A>C
ENST00000215730.11:c.*507A>C ENSP00000215730.6:n.*507A>C
NM_004782.3:c.*507A>C NP_004773.1:n.*507A>C
NM_004782.4:c.*507A>C MANE Select NP_004773.1:n.*507A>C
Search 100 bp 5'
Search 100 bp 3'