Canonical Allele Identifier: CA2655449185
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888018G>A , CM000684.2:g.20888018G>A GRCh38
NC_000022.10:g.21242306G>A , CM000684.1:g.21242306G>A GRCh37
NC_000022.9:g.19572306G>A NCBI36
NG_012152.1:g.34015G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*182G>A MANE Select ENSP00000215730.6:n.*182G>A
ENST00000215730.11:c.*182G>A ENSP00000215730.6:n.*182G>A
NM_004782.3:c.*182G>A NP_004773.1:n.*182G>A
NM_004782.4:c.*182G>A MANE Select NP_004773.1:n.*182G>A