Canonical Allele Identifier: CA14446988
Gene: LGALS9DP HGNC NCBI
COSMIC:
COSN8866161 (not active)
MyVariant.info:
GRCh38 chr17:g.27748474T>C
GRCh37 chr17:g.26075500T>C
gnomAD v2:
17:26075500 T / C
gnomAD v3:
17:27748474 T / C
gnomAD v4:
chr17-27748474-T-C
Joint Max Group AF 0.74609158 (AFR)
Genomes Max Group AF 0.74538303 (AFR)
Exomes Max Group AF 0.73752853 (AFR)
dbSNP:
7215373
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27748474T>C , CM000679.2:g.27748474T>C GRCh38
NC_000017.10:g.26075500T>C , CM000679.1:g.26075500T>C GRCh37
NC_000017.9:g.23099627T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000580112.1:n.317+146T>C
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