ClinGen Allele Registry
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Canonical Allele Identifier:
CA832620958
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.122990126A>T
GRCh37
chr7:g.122630180A>T
Linked Data - NCBI & NCI
dbSNP:
846672
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.122990126A>T , CM000669.2:g.122990126A>T
GRCh38
NC_000007.13:g.122630180A>T , CM000669.1:g.122630180A>T
GRCh37
NC_000007.12:g.122417416A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'