Canonical Allele Identifier: CA2655449533
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888491-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888491T>C , CM000684.2:g.20888491T>C GRCh38
NC_000022.10:g.21242779T>C , CM000684.1:g.21242779T>C GRCh37
NC_000022.9:g.19572779T>C NCBI36
NG_012152.1:g.34488T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*655T>C MANE Select ENSP00000215730.6:n.*655T>C
ENST00000215730.11:c.*655T>C ENSP00000215730.6:n.*655T>C
NM_004782.3:c.*655T>C NP_004773.1:n.*655T>C
NM_004782.4:c.*655T>C MANE Select NP_004773.1:n.*655T>C
Search 100 bp 5'
Search 100 bp 3'