Canonical Allele Identifier: CA2655449178
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888005C>A , CM000684.2:g.20888005C>A GRCh38
NC_000022.10:g.21242293C>A , CM000684.1:g.21242293C>A GRCh37
NC_000022.9:g.19572293C>A NCBI36
NG_012152.1:g.34002C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*169C>A MANE Select ENSP00000215730.6:n.*169C>A
ENST00000215730.11:c.*169C>A ENSP00000215730.6:n.*169C>A
NM_004782.3:c.*169C>A NP_004773.1:n.*169C>A
NM_004782.4:c.*169C>A MANE Select NP_004773.1:n.*169C>A