Canonical Allele Identifier: CA322277851
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs939242951
gnomAD v3: 22-20888530-C-G
gnomAD v4: 22-20888530-C-G
MyVariant Identifiers: chr22:g.21242818C>G (hg19) chr22:g.20888530C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888530C>G , CM000684.2:g.20888530C>G GRCh38
NC_000022.10:g.21242818C>G , CM000684.1:g.21242818C>G GRCh37
NC_000022.9:g.19572818C>G NCBI36
NG_012152.1:g.34527C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*694C>G MANE Select ENSP00000215730.6:n.*694C>G
ENST00000215730.11:c.*694C>G ENSP00000215730.6:n.*694C>G
NM_004782.3:c.*694C>G NP_004773.1:n.*694C>G
NM_004782.4:c.*694C>G MANE Select NP_004773.1:n.*694C>G
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