Canonical Allele Identifier: CA751562876
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1159319718

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888204A>G , CM000684.2:g.20888204A>G GRCh38
NC_000022.10:g.21242492A>G , CM000684.1:g.21242492A>G GRCh37
NC_000022.9:g.19572492A>G NCBI36
NG_012152.1:g.34201A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*368A>G MANE Select ENSP00000215730.6:n.*368A>G
ENST00000215730.11:c.*368A>G ENSP00000215730.6:n.*368A>G
NM_004782.3:c.*368A>G NP_004773.1:n.*368A>G
NM_004782.4:c.*368A>G MANE Select NP_004773.1:n.*368A>G