ClinGen Allele Registry
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Canonical Allele Identifier:
CA607414939
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.102731912G>T
GRCh37
chr12:g.103125690G>T
Linked Data - Sequence & Population
gnomAD v2:
12:103125690 G / T
gnomAD v3:
12:102731912 G / T
gnomAD v4:
chr12-102731912-G-T
Linked Data - NCBI & NCI
dbSNP:
2172873
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.102731912G>T , CM000674.2:g.102731912G>T
GRCh38
NC_000012.11:g.103125690G>T , CM000674.1:g.103125690G>T
GRCh37
NC_000012.10:g.101649820G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'