Canonical Allele Identifier: CA322277415
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1052023587
gnomAD v4: 22-20887935-T-G
MyVariant Identifiers: chr22:g.21242223T>G (hg19) chr22:g.20887935T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20887935T>G , CM000684.2:g.20887935T>G GRCh38
NC_000022.10:g.21242223T>G , CM000684.1:g.21242223T>G GRCh37
NC_000022.9:g.19572223T>G NCBI36
NG_012152.1:g.33932T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*99T>G MANE Select ENSP00000215730.6:n.*99T>G
ENST00000215730.11:c.*99T>G ENSP00000215730.6:n.*99T>G
NM_004782.3:c.*99T>G NP_004773.1:n.*99T>G
NM_004782.4:c.*99T>G MANE Select NP_004773.1:n.*99T>G
Search 100 bp 5'
Search 100 bp 3'