Canonical Allele Identifier: CA2655449332
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888301-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888301G>T , CM000684.2:g.20888301G>T GRCh38
NC_000022.10:g.21242589G>T , CM000684.1:g.21242589G>T GRCh37
NC_000022.9:g.19572589G>T NCBI36
NG_012152.1:g.34298G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*465G>T MANE Select ENSP00000215730.6:n.*465G>T
ENST00000215730.11:c.*465G>T ENSP00000215730.6:n.*465G>T
NM_004782.3:c.*465G>T NP_004773.1:n.*465G>T
NM_004782.4:c.*465G>T MANE Select NP_004773.1:n.*465G>T
Search 100 bp 5'
Search 100 bp 3'