Canonical Allele Identifier: CA2396589508
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1601657181
gnomAD v4: 22-20888199-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888199C>A , CM000684.2:g.20888199C>A GRCh38
NC_000022.10:g.21242487C>A , CM000684.1:g.21242487C>A GRCh37
NC_000022.9:g.19572487C>A NCBI36
NG_012152.1:g.34196C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*363C>A MANE Select ENSP00000215730.6:n.*363C>A
ENST00000215730.11:c.*363C>A ENSP00000215730.6:n.*363C>A
NM_004782.3:c.*363C>A NP_004773.1:n.*363C>A
NM_004782.4:c.*363C>A MANE Select NP_004773.1:n.*363C>A
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