Canonical Allele Identifier: CA2655449347
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888313-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888313A>C , CM000684.2:g.20888313A>C GRCh38
NC_000022.10:g.21242601A>C , CM000684.1:g.21242601A>C GRCh37
NC_000022.9:g.19572601A>C NCBI36
NG_012152.1:g.34310A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*477A>C MANE Select ENSP00000215730.6:n.*477A>C
ENST00000215730.11:c.*477A>C ENSP00000215730.6:n.*477A>C
NM_004782.3:c.*477A>C NP_004773.1:n.*477A>C
NM_004782.4:c.*477A>C MANE Select NP_004773.1:n.*477A>C
Search 100 bp 5'
Search 100 bp 3'