Canonical Allele Identifier: CA10653870
Gene: SNAP29 HGNC NCBI

Linked Data

ClinVar Variation Id: 340841
ClinVar RCV Id: RCV000375091
dbSNP Id: rs187586025

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888091G>A , CM000684.2:g.20888091G>A GRCh38
NC_000022.10:g.21242379G>A , CM000684.1:g.21242379G>A GRCh37
NC_000022.9:g.19572379G>A NCBI36
NG_012152.1:g.34088G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*255G>A MANE Select ENSP00000215730.6:n.*255G>A
ENST00000215730.11:c.*255G>A ENSP00000215730.6:n.*255G>A
NM_004782.3:c.*255G>A NP_004773.1:n.*255G>A
NM_004782.4:c.*255G>A MANE Select NP_004773.1:n.*255G>A