Canonical Allele Identifier: CA751562938
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1430852091
gnomAD v3: 22-20888525-C-T
gnomAD v4: 22-20888525-C-T
MyVariant Identifiers: chr22:g.21242813C>T (hg19) chr22:g.20888525C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888525C>T , CM000684.2:g.20888525C>T GRCh38
NC_000022.10:g.21242813C>T , CM000684.1:g.21242813C>T GRCh37
NC_000022.9:g.19572813C>T NCBI36
NG_012152.1:g.34522C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*689C>T MANE Select ENSP00000215730.6:n.*689C>T
ENST00000215730.11:c.*689C>T ENSP00000215730.6:n.*689C>T
NM_004782.3:c.*689C>T NP_004773.1:n.*689C>T
NM_004782.4:c.*689C>T MANE Select NP_004773.1:n.*689C>T
Search 100 bp 5'
Search 100 bp 3'