Canonical Allele Identifier: CA638542855
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1196580347
gnomAD v2: 22-21242819-G-A
gnomAD v3: 22-20888531-G-A
gnomAD v4: 22-20888531-G-A
MyVariant Identifiers: chr22:g.21242819G>A (hg19) chr22:g.20888531G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888531G>A , CM000684.2:g.20888531G>A GRCh38
NC_000022.10:g.21242819G>A , CM000684.1:g.21242819G>A GRCh37
NC_000022.9:g.19572819G>A NCBI36
NG_012152.1:g.34528G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*695G>A MANE Select ENSP00000215730.6:n.*695G>A
ENST00000215730.11:c.*695G>A ENSP00000215730.6:n.*695G>A
NM_004782.3:c.*695G>A NP_004773.1:n.*695G>A
NM_004782.4:c.*695G>A MANE Select NP_004773.1:n.*695G>A
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