Canonical Allele Identifier: CA322277406
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs3202072
MyVariant Identifiers: chr22:g.21242189G>A (hg19) chr22:g.20887901G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20887901G>A , CM000684.2:g.20887901G>A GRCh38
NC_000022.10:g.21242189G>A , CM000684.1:g.21242189G>A GRCh37
NC_000022.9:g.19572189G>A NCBI36
NG_012152.1:g.33898G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*65G>A MANE Select ENSP00000215730.6:n.*65G>A
ENST00000215730.11:c.*65G>A ENSP00000215730.6:n.*65G>A
NM_004782.3:c.*65G>A NP_004773.1:n.*65G>A
NM_004782.4:c.*65G>A MANE Select NP_004773.1:n.*65G>A
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