Canonical Allele Identifier: CA2655449560
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888518-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888518C>T , CM000684.2:g.20888518C>T GRCh38
NC_000022.10:g.21242806C>T , CM000684.1:g.21242806C>T GRCh37
NC_000022.9:g.19572806C>T NCBI36
NG_012152.1:g.34515C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*682C>T MANE Select ENSP00000215730.6:n.*682C>T
ENST00000215730.11:c.*682C>T ENSP00000215730.6:n.*682C>T
NM_004782.3:c.*682C>T NP_004773.1:n.*682C>T
NM_004782.4:c.*682C>T MANE Select NP_004773.1:n.*682C>T
Search 100 bp 5'
Search 100 bp 3'