Canonical Allele Identifier: CA2655449221
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888082-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888082C>A , CM000684.2:g.20888082C>A GRCh38
NC_000022.10:g.21242370C>A , CM000684.1:g.21242370C>A GRCh37
NC_000022.9:g.19572370C>A NCBI36
NG_012152.1:g.34079C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*246C>A MANE Select ENSP00000215730.6:n.*246C>A
ENST00000215730.11:c.*246C>A ENSP00000215730.6:n.*246C>A
NM_004782.3:c.*246C>A NP_004773.1:n.*246C>A
NM_004782.4:c.*246C>A MANE Select NP_004773.1:n.*246C>A
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