ClinGen Allele Registry
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Canonical Allele Identifier:
CA601776862
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.113407963G>C
GRCh37
chr11:g.113278685G>C
Linked Data - Sequence & Population
gnomAD v2:
11:113278685 G / C
gnomAD v3:
11:113407963 G / C
gnomAD v4:
chr11-113407963-G-C
Linked Data - NCBI & NCI
dbSNP:
1309691247
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.113407963G>C , CM000673.2:g.113407963G>C
GRCh38
NC_000011.9:g.113278685G>C , CM000673.1:g.113278685G>C
GRCh37
NC_000011.8:g.112783895G>C
NCBI36
NG_008841.1:g.72317C>G
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