Canonical Allele Identifier: CA1024230449
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929067977
gnomAD v3: 22-20888298-T-G
gnomAD v4: 22-20888298-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888298T>G , CM000684.2:g.20888298T>G GRCh38
NC_000022.10:g.21242586T>G , CM000684.1:g.21242586T>G GRCh37
NC_000022.9:g.19572586T>G NCBI36
NG_012152.1:g.34295T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*462T>G MANE Select ENSP00000215730.6:n.*462T>G
ENST00000215730.11:c.*462T>G ENSP00000215730.6:n.*462T>G
NM_004782.3:c.*462T>G NP_004773.1:n.*462T>G
NM_004782.4:c.*462T>G MANE Select NP_004773.1:n.*462T>G
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