Canonical Allele Identifier: CA196508968

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs972211032
• MyVariant Identifiers: chr9:g.96929449T>C (hg19) ; chr9:g.94167167T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167167T>C , CM000671.2:g.94167167T>C	GRCh38
NC_000009.11:g.96929449T>C , CM000671.1:g.96929449T>C	GRCh37
NC_000009.10:g.95969270T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+786T>C
NR_170275.1:n.124+786T>C
NR_170276.1:n.124+786T>C
NR_170277.1:n.124+786T>C
NR_170278.1:n.124+786T>C