Canonical Allele Identifier: CA751562927
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1207549743
gnomAD v3: 22-20888477-C-G
gnomAD v4: 22-20888477-C-G
MyVariant Identifiers: chr22:g.21242765C>G (hg19) chr22:g.20888477C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888477C>G , CM000684.2:g.20888477C>G GRCh38
NC_000022.10:g.21242765C>G , CM000684.1:g.21242765C>G GRCh37
NC_000022.9:g.19572765C>G NCBI36
NG_012152.1:g.34474C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*641C>G MANE Select ENSP00000215730.6:n.*641C>G
ENST00000215730.11:c.*641C>G ENSP00000215730.6:n.*641C>G
NM_004782.3:c.*641C>G NP_004773.1:n.*641C>G
NM_004782.4:c.*641C>G MANE Select NP_004773.1:n.*641C>G
Search 100 bp 5'
Search 100 bp 3'