Canonical Allele Identifier: CA2396589699
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1601657464
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888486G>A , CM000684.2:g.20888486G>A GRCh38
NC_000022.10:g.21242774G>A , CM000684.1:g.21242774G>A GRCh37
NC_000022.9:g.19572774G>A NCBI36
NG_012152.1:g.34483G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*650G>A MANE Select ENSP00000215730.6:n.*650G>A
ENST00000215730.11:c.*650G>A ENSP00000215730.6:n.*650G>A
NM_004782.3:c.*650G>A NP_004773.1:n.*650G>A
NM_004782.4:c.*650G>A MANE Select NP_004773.1:n.*650G>A
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