Canonical Allele Identifier: CA751562926
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1485902199
gnomAD v4: 22-20888472-G-GC
MyVariant Identifiers: chr22:g.21242760_21242761insC (hg19) chr22:g.20888472_20888473insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888478dup , CM000684.2:g.20888478dup GRCh38
NC_000022.10:g.21242766dup , CM000684.1:g.21242766dup GRCh37
NC_000022.9:g.19572766dup NCBI36
NG_012152.1:g.34475dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*642dup MANE Select ENSP00000215730.6:n.*642dup
ENST00000215730.11:c.*642dup ENSP00000215730.6:n.*642dup
NM_004782.3:c.*642dup NP_004773.1:n.*642dup
NM_004782.4:c.*642dup MANE Select NP_004773.1:n.*642dup
Search 100 bp 5'
Search 100 bp 3'