Canonical Allele Identifier: CA2655449190
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888025A>T , CM000684.2:g.20888025A>T GRCh38
NC_000022.10:g.21242313A>T , CM000684.1:g.21242313A>T GRCh37
NC_000022.9:g.19572313A>T NCBI36
NG_012152.1:g.34022A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*189A>T MANE Select ENSP00000215730.6:n.*189A>T
ENST00000215730.11:c.*189A>T ENSP00000215730.6:n.*189A>T
NM_004782.3:c.*189A>T NP_004773.1:n.*189A>T
NM_004782.4:c.*189A>T MANE Select NP_004773.1:n.*189A>T