Canonical Allele Identifier: CA1024230781
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929078473
gnomAD v3: 22-20888488-A-G
gnomAD v4: 22-20888488-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888488A>G , CM000684.2:g.20888488A>G GRCh38
NC_000022.10:g.21242776A>G , CM000684.1:g.21242776A>G GRCh37
NC_000022.9:g.19572776A>G NCBI36
NG_012152.1:g.34485A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*652A>G MANE Select ENSP00000215730.6:n.*652A>G
ENST00000215730.11:c.*652A>G ENSP00000215730.6:n.*652A>G
NM_004782.3:c.*652A>G NP_004773.1:n.*652A>G
NM_004782.4:c.*652A>G MANE Select NP_004773.1:n.*652A>G
Search 100 bp 5'
Search 100 bp 3'