Canonical Allele Identifier: CA2396589465
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929063514
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888088C>T , CM000684.2:g.20888088C>T GRCh38
NC_000022.10:g.21242376C>T , CM000684.1:g.21242376C>T GRCh37
NC_000022.9:g.19572376C>T NCBI36
NG_012152.1:g.34085C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*252C>T MANE Select ENSP00000215730.6:n.*252C>T
ENST00000215730.11:c.*252C>T ENSP00000215730.6:n.*252C>T
NM_004782.3:c.*252C>T NP_004773.1:n.*252C>T
NM_004782.4:c.*252C>T MANE Select NP_004773.1:n.*252C>T
Search 100 bp 5'
Search 100 bp 3'