Canonical Allele Identifier: CA589477139

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs1372137000
• gnomAD v2: 9-96929669-G-A
• gnomAD v3: 9-94167387-G-A
• gnomAD v4: 9-94167387-G-A
• MyVariant Identifiers: chr9:g.96929669G>A (hg19) ; chr9:g.94167387G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167387G>A , CM000671.2:g.94167387G>A	GRCh38
NC_000009.11:g.96929669G>A , CM000671.1:g.96929669G>A	GRCh37
NC_000009.10:g.95969490G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+1006G>A
NR_170275.1:n.124+1006G>A
NR_170276.1:n.124+1006G>A
NR_170277.1:n.124+1006G>A
NR_170278.1:n.124+1006G>A