Canonical Allele Identifier: CA2655449545
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888506-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888506G>A , CM000684.2:g.20888506G>A GRCh38
NC_000022.10:g.21242794G>A , CM000684.1:g.21242794G>A GRCh37
NC_000022.9:g.19572794G>A NCBI36
NG_012152.1:g.34503G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*670G>A MANE Select ENSP00000215730.6:n.*670G>A
ENST00000215730.11:c.*670G>A ENSP00000215730.6:n.*670G>A
NM_004782.3:c.*670G>A NP_004773.1:n.*670G>A
NM_004782.4:c.*670G>A MANE Select NP_004773.1:n.*670G>A
Search 100 bp 5'
Search 100 bp 3'