Canonical Allele Identifier: CA2396589708
Gene: SNAP29 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888508T= , CM000684.2:g.20888508T= GRCh38
NC_000022.10:g.21242796T= , CM000684.1:g.21242796T= GRCh37
NC_000022.9:g.19572796T= NCBI36
NG_012152.1:g.34505T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*672T= MANE Select ENSP00000215730.6:n.*672T=
ENST00000215730.11:c.*672T= ENSP00000215730.6:n.*672T=
NM_004782.3:c.*672T= NP_004773.1:n.*672T=
NM_004782.4:c.*672T= MANE Select NP_004773.1:n.*672T=
Search 100 bp 5'
Search 100 bp 3'