ClinGen Allele Registry
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Canonical Allele Identifier:
CA147948984
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.131956291C>T
GRCh37
chr6:g.132277431C>T
Linked Data - NCBI & NCI
dbSNP:
9402373
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.131956291C>T , CM000668.2:g.131956291C>T
GRCh38
NC_000006.11:g.132277431C>T , CM000668.1:g.132277431C>T
GRCh37
NC_000006.10:g.132319124C>T
NCBI36
NG_016131.1:g.88G>A
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