ClinGen Allele Registry
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Canonical Allele Identifier:
CA13674063
Gene: DRAM1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.101928157G>A
GRCh37
chr12:g.102321935G>A
Linked Data - Sequence & Population
gnomAD v2:
12:102321935 G / A
gnomAD v3:
12:101928157 G / A
gnomAD v4:
chr12-101928157-G-A
Joint Max Group AF
0.64402437 (AFR)
Genomes Max Group AF
0.64402437 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4622329
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.101928157G>A , CM000674.2:g.101928157G>A
GRCh38
NC_000012.11:g.102321935G>A , CM000674.1:g.102321935G>A
GRCh37
NC_000012.10:g.100846066G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000549066.1:c.109+13925G>A
Search 100 bp 5'
Search 100 bp 3'