Allele Registry

Canonical Allele Identifier: CA673452051

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.130947684T>C

GRCh37 chr11:g.130817579T>C

Linked Data - Sequence & Population

gnomAD v3:

11:130947684 T / C

gnomAD v4:

chr11-130947684-T-C

Linked Data - NCBI & NCI

dbSNP:

7940866

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130947684T>C , CM000673.2:g.130947684T>C	GRCh38
NC_000011.9:g.130817579T>C , CM000673.1:g.130817579T>C	GRCh37
NC_000011.8:g.130322789T>C	NCBI36

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