Canonical Allele Identifier: CA2655449187
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888021T>C , CM000684.2:g.20888021T>C GRCh38
NC_000022.10:g.21242309T>C , CM000684.1:g.21242309T>C GRCh37
NC_000022.9:g.19572309T>C NCBI36
NG_012152.1:g.34018T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*185T>C MANE Select ENSP00000215730.6:n.*185T>C
ENST00000215730.11:c.*185T>C ENSP00000215730.6:n.*185T>C
NM_004782.3:c.*185T>C NP_004773.1:n.*185T>C
NM_004782.4:c.*185T>C MANE Select NP_004773.1:n.*185T>C