Canonical Allele Identifier: CA10653240
Gene: SNAP29 HGNC NCBI

Linked Data

ClinVar Variation Id: 340872
ClinVar RCV Id: RCV000361373
dbSNP Id: rs74557072

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20889888A>T , CM000684.2:g.20889888A>T GRCh38
NC_000022.10:g.21244176A>T , CM000684.1:g.21244176A>T GRCh37
NC_000022.9:g.19574176A>T NCBI36
NG_012152.1:g.35885A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*2052A>T MANE Select ENSP00000215730.6:n.*2052A>T
ENST00000215730.11:c.*2052A>T ENSP00000215730.6:n.*2052A>T
NM_004782.3:c.*2052A>T NP_004773.1:n.*2052A>T
NM_004782.4:c.*2052A>T MANE Select NP_004773.1:n.*2052A>T