Canonical Allele Identifier: CA2396589488
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929064701

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888136C>T , CM000684.2:g.20888136C>T GRCh38
NC_000022.10:g.21242424C>T , CM000684.1:g.21242424C>T GRCh37
NC_000022.9:g.19572424C>T NCBI36
NG_012152.1:g.34133C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*300C>T MANE Select ENSP00000215730.6:n.*300C>T
ENST00000215730.11:c.*300C>T ENSP00000215730.6:n.*300C>T
NM_004782.3:c.*300C>T NP_004773.1:n.*300C>T
NM_004782.4:c.*300C>T MANE Select NP_004773.1:n.*300C>T