Canonical Allele Identifier: CA2738111827
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs2147875290
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888384dup , CM000684.2:g.20888384dup GRCh38
NC_000022.10:g.21242672dup , CM000684.1:g.21242672dup GRCh37
NC_000022.9:g.19572672dup NCBI36
NG_012152.1:g.34381dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*548dup MANE Select ENSP00000215730.6:n.*548dup
ENST00000215730.11:c.*548dup ENSP00000215730.6:n.*548dup
NM_004782.3:c.*548dup NP_004773.1:n.*548dup
NM_004782.4:c.*548dup MANE Select NP_004773.1:n.*548dup
Search 100 bp 5'
Search 100 bp 3'