Canonical Allele Identifier: CA10653881
Gene: SNAP29 HGNC NCBI

Linked Data

ClinVar Variation Id: 340854
ClinVar RCV Id: RCV000300230
dbSNP Id: rs361998
gnomAD v2: 22-21242645-T-A
gnomAD v3: 22-20888357-T-A
gnomAD v4: 22-20888357-T-A
MyVariant Identifiers: chr22:g.21242645T>A (hg19) chr22:g.20888357T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888357T>A , CM000684.2:g.20888357T>A GRCh38
NC_000022.10:g.21242645T>A , CM000684.1:g.21242645T>A GRCh37
NC_000022.9:g.19572645T>A NCBI36
NG_012152.1:g.34354T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*521T>A MANE Select ENSP00000215730.6:n.*521T>A
ENST00000215730.11:c.*521T>A ENSP00000215730.6:n.*521T>A
NM_004782.3:c.*521T>A NP_004773.1:n.*521T>A
NM_004782.4:c.*521T>A MANE Select NP_004773.1:n.*521T>A
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Search 100 bp 3'