Canonical Allele Identifier: CA322277447
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs961045700

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888016A>G , CM000684.2:g.20888016A>G GRCh38
NC_000022.10:g.21242304A>G , CM000684.1:g.21242304A>G GRCh37
NC_000022.9:g.19572304A>G NCBI36
NG_012152.1:g.34013A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*180A>G MANE Select ENSP00000215730.6:n.*180A>G
ENST00000215730.11:c.*180A>G ENSP00000215730.6:n.*180A>G
NM_004782.3:c.*180A>G NP_004773.1:n.*180A>G
NM_004782.4:c.*180A>G MANE Select NP_004773.1:n.*180A>G