Canonical Allele Identifier: CA2396589489
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888145T= , CM000684.2:g.20888145T= GRCh38
NC_000022.10:g.21242433T= , CM000684.1:g.21242433T= GRCh37
NC_000022.9:g.19572433T= NCBI36
NG_012152.1:g.34142T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*309T= MANE Select ENSP00000215730.6:n.*309T=
ENST00000215730.11:c.*309T= ENSP00000215730.6:n.*309T=
NM_004782.3:c.*309T= NP_004773.1:n.*309T=
NM_004782.4:c.*309T= MANE Select NP_004773.1:n.*309T=
Search 100 bp 5'
Search 100 bp 3'