Canonical Allele Identifier: CA2655449546
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888506-G-T
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*670G>T MANE Select ENSP00000215730.6:n.*670G>T
ENST00000215730.11:c.*670G>T ENSP00000215730.6:n.*670G>T
NM_004782.3:c.*670G>T NP_004773.1:n.*670G>T
NM_004782.4:c.*670G>T MANE Select NP_004773.1:n.*670G>T
Search 100 bp 5'
Search 100 bp 3'