Canonical Allele Identifier: CA2396589702
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888492A= , CM000684.2:g.20888492A= GRCh38
NC_000022.10:g.21242780A= , CM000684.1:g.21242780A= GRCh37
NC_000022.9:g.19572780A= NCBI36
NG_012152.1:g.34489A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*656A= MANE Select ENSP00000215730.6:n.*656A=
ENST00000215730.11:c.*656A= ENSP00000215730.6:n.*656A=
NM_004782.3:c.*656A= NP_004773.1:n.*656A=
NM_004782.4:c.*656A= MANE Select NP_004773.1:n.*656A=
Search 100 bp 5'
Search 100 bp 3'