Canonical Allele Identifier: CA10974919
Gene: MIR29B2CHG HGNC NCBI

Linked Data

dbSNP Id: rs1967689
gnomAD v2: 1-208039471-G-C
gnomAD v3: 1-207866126-G-C
gnomAD v4: 1-207866126-G-C
MyVariant Identifiers: chr1:g.208039471G>C (hg19) chr1:g.207866126G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207866126G>C , CM000663.2:g.207866126G>C GRCh38
NC_000001.10:g.208039471G>C , CM000663.1:g.208039471G>C GRCh37
NC_000001.9:g.206106094G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922491.1:n.143+1800C>G
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