Canonical Allele Identifier: CA2655449267
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888222T>C , CM000684.2:g.20888222T>C GRCh38
NC_000022.10:g.21242510T>C , CM000684.1:g.21242510T>C GRCh37
NC_000022.9:g.19572510T>C NCBI36
NG_012152.1:g.34219T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*386T>C MANE Select ENSP00000215730.6:n.*386T>C
ENST00000215730.11:c.*386T>C ENSP00000215730.6:n.*386T>C
NM_004782.3:c.*386T>C NP_004773.1:n.*386T>C
NM_004782.4:c.*386T>C MANE Select NP_004773.1:n.*386T>C