ClinGen Allele Registry
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Canonical Allele Identifier:
CA303995937
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1106943G>C
GRCh37
chr19:g.1106942G>C
Linked Data - Sequence & Population
gnomAD v3:
19:1106943 G / C
gnomAD v4:
chr19-1106943-G-C
Linked Data - NCBI & NCI
dbSNP:
978216230
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1106943G>C , CM000681.2:g.1106943G>C
GRCh38
NC_000019.9:g.1106942G>C , CM000681.1:g.1106942G>C
GRCh37
NC_000019.8:g.1057942G>C
NCBI36
NG_050621.1:g.8018G>C
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