Canonical Allele Identifier: CA2655449177
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888004C>A , CM000684.2:g.20888004C>A GRCh38
NC_000022.10:g.21242292C>A , CM000684.1:g.21242292C>A GRCh37
NC_000022.9:g.19572292C>A NCBI36
NG_012152.1:g.34001C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*168C>A MANE Select ENSP00000215730.6:n.*168C>A
ENST00000215730.11:c.*168C>A ENSP00000215730.6:n.*168C>A
NM_004782.3:c.*168C>A NP_004773.1:n.*168C>A
NM_004782.4:c.*168C>A MANE Select NP_004773.1:n.*168C>A