Canonical Allele Identifier: CA751562933
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1301215888
MyVariant Identifiers: chr22:g.21242796T>G (hg19) chr22:g.20888508T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888508T>G , CM000684.2:g.20888508T>G GRCh38
NC_000022.10:g.21242796T>G , CM000684.1:g.21242796T>G GRCh37
NC_000022.9:g.19572796T>G NCBI36
NG_012152.1:g.34505T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*672T>G MANE Select ENSP00000215730.6:n.*672T>G
ENST00000215730.11:c.*672T>G ENSP00000215730.6:n.*672T>G
NM_004782.3:c.*672T>G NP_004773.1:n.*672T>G
NM_004782.4:c.*672T>G MANE Select NP_004773.1:n.*672T>G
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