Canonical Allele Identifier: CA2655449420
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888375-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888375G>C , CM000684.2:g.20888375G>C GRCh38
NC_000022.10:g.21242663G>C , CM000684.1:g.21242663G>C GRCh37
NC_000022.9:g.19572663G>C NCBI36
NG_012152.1:g.34372G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*539G>C MANE Select ENSP00000215730.6:n.*539G>C
ENST00000215730.11:c.*539G>C ENSP00000215730.6:n.*539G>C
NM_004782.3:c.*539G>C NP_004773.1:n.*539G>C
NM_004782.4:c.*539G>C MANE Select NP_004773.1:n.*539G>C
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