Canonical Allele Identifier: CA2655449246
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888160-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888160G>T , CM000684.2:g.20888160G>T GRCh38
NC_000022.10:g.21242448G>T , CM000684.1:g.21242448G>T GRCh37
NC_000022.9:g.19572448G>T NCBI36
NG_012152.1:g.34157G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*324G>T MANE Select ENSP00000215730.6:n.*324G>T
ENST00000215730.11:c.*324G>T ENSP00000215730.6:n.*324G>T
NM_004782.3:c.*324G>T NP_004773.1:n.*324G>T
NM_004782.4:c.*324G>T MANE Select NP_004773.1:n.*324G>T
Search 100 bp 5'
Search 100 bp 3'