Canonical Allele Identifier: CA2655449235
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888119-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888119T>A , CM000684.2:g.20888119T>A GRCh38
NC_000022.10:g.21242407T>A , CM000684.1:g.21242407T>A GRCh37
NC_000022.9:g.19572407T>A NCBI36
NG_012152.1:g.34116T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*283T>A MANE Select ENSP00000215730.6:n.*283T>A
ENST00000215730.11:c.*283T>A ENSP00000215730.6:n.*283T>A
NM_004782.3:c.*283T>A NP_004773.1:n.*283T>A
NM_004782.4:c.*283T>A MANE Select NP_004773.1:n.*283T>A
Search 100 bp 5'
Search 100 bp 3'