Canonical Allele Identifier: CA751562922
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1480082382
gnomAD v3: 22-20888443-T-C
gnomAD v4: 22-20888443-T-C
MyVariant Identifiers: chr22:g.21242731T>C (hg19) chr22:g.20888443T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888443T>C , CM000684.2:g.20888443T>C GRCh38
NC_000022.10:g.21242731T>C , CM000684.1:g.21242731T>C GRCh37
NC_000022.9:g.19572731T>C NCBI36
NG_012152.1:g.34440T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*607T>C MANE Select ENSP00000215730.6:n.*607T>C
ENST00000215730.11:c.*607T>C ENSP00000215730.6:n.*607T>C
NM_004782.3:c.*607T>C NP_004773.1:n.*607T>C
NM_004782.4:c.*607T>C MANE Select NP_004773.1:n.*607T>C
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