Canonical Allele Identifier: CA322277503
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1012021392
gnomAD v3: 22-20888117-G-T
gnomAD v4: 22-20888117-G-T
MyVariant Identifiers: chr22:g.21242405G>T (hg19) chr22:g.20888117G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888117G>T , CM000684.2:g.20888117G>T GRCh38
NC_000022.10:g.21242405G>T , CM000684.1:g.21242405G>T GRCh37
NC_000022.9:g.19572405G>T NCBI36
NG_012152.1:g.34114G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*281G>T MANE Select ENSP00000215730.6:n.*281G>T
ENST00000215730.11:c.*281G>T ENSP00000215730.6:n.*281G>T
NM_004782.3:c.*281G>T NP_004773.1:n.*281G>T
NM_004782.4:c.*281G>T MANE Select NP_004773.1:n.*281G>T
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Search 100 bp 3'