Canonical Allele Identifier: CA196509012

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs901655372
• MyVariant Identifiers: chr9:g.96929549T>C (hg19) ; chr9:g.94167267T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167267T>C , CM000671.2:g.94167267T>C	GRCh38
NC_000009.11:g.96929549T>C , CM000671.1:g.96929549T>C	GRCh37
NC_000009.10:g.95969370T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+886T>C
NR_170275.1:n.124+886T>C
NR_170276.1:n.124+886T>C
NR_170277.1:n.124+886T>C
NR_170278.1:n.124+886T>C