Canonical Allele Identifier: CA2396590067
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20889387G= , CM000684.2:g.20889387G= GRCh38
NC_000022.10:g.21243675G= , CM000684.1:g.21243675G= GRCh37
NC_000022.9:g.19573675G= NCBI36
NG_012152.1:g.35384G=

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*1551G= MANE Select ENSP00000215730.6:n.*1551G=
ENST00000215730.11:c.*1551G= ENSP00000215730.6:n.*1551G=
NM_004782.3:c.*1551G= NP_004773.1:n.*1551G=
NM_004782.4:c.*1551G= MANE Select NP_004773.1:n.*1551G=
Search 100 bp 5'
Search 100 bp 3'