Canonical Allele Identifier: CA1024231012
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929099206
gnomAD v3: 22-20889436-T-C
gnomAD v4: 22-20889436-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20889436T>C , CM000684.2:g.20889436T>C GRCh38
NC_000022.10:g.21243724T>C , CM000684.1:g.21243724T>C GRCh37
NC_000022.9:g.19573724T>C NCBI36
NG_012152.1:g.35433T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*1600T>C MANE Select ENSP00000215730.6:n.*1600T>C
ENST00000215730.11:c.*1600T>C ENSP00000215730.6:n.*1600T>C
NM_004782.3:c.*1600T>C NP_004773.1:n.*1600T>C
NM_004782.4:c.*1600T>C MANE Select NP_004773.1:n.*1600T>C
Search 100 bp 5'
Search 100 bp 3'