Canonical Allele Identifier: CA322277577
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1019156033
gnomAD v4: 22-20888299-A-G
MyVariant Identifiers: chr22:g.21242587A>G (hg19) chr22:g.20888299A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888299A>G , CM000684.2:g.20888299A>G GRCh38
NC_000022.10:g.21242587A>G , CM000684.1:g.21242587A>G GRCh37
NC_000022.9:g.19572587A>G NCBI36
NG_012152.1:g.34296A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*463A>G MANE Select ENSP00000215730.6:n.*463A>G
ENST00000215730.11:c.*463A>G ENSP00000215730.6:n.*463A>G
NM_004782.3:c.*463A>G NP_004773.1:n.*463A>G
NM_004782.4:c.*463A>G MANE Select NP_004773.1:n.*463A>G
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