Canonical Allele Identifier: CA2738111844
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs2147875313
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888423G>C , CM000684.2:g.20888423G>C GRCh38
NC_000022.10:g.21242711G>C , CM000684.1:g.21242711G>C GRCh37
NC_000022.9:g.19572711G>C NCBI36
NG_012152.1:g.34420G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*587G>C MANE Select ENSP00000215730.6:n.*587G>C
ENST00000215730.11:c.*587G>C ENSP00000215730.6:n.*587G>C
NM_004782.3:c.*587G>C NP_004773.1:n.*587G>C
NM_004782.4:c.*587G>C MANE Select NP_004773.1:n.*587G>C
Search 100 bp 5'
Search 100 bp 3'