ClinGen Allele Registry
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Canonical Allele Identifier:
CA303995941
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1106946G>C
GRCh37
chr19:g.1106945G>C
Linked Data - Sequence & Population
gnomAD v3:
19:1106946 G / C
gnomAD v4:
chr19-1106946-G-C
Linked Data - NCBI & NCI
dbSNP:
936814920
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1106946G>C , CM000681.2:g.1106946G>C
GRCh38
NC_000019.9:g.1106945G>C , CM000681.1:g.1106945G>C
GRCh37
NC_000019.8:g.1057945G>C
NCBI36
NG_050621.1:g.8021G>C
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