Canonical Allele Identifier: CA196509097

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs977928198
• MyVariant Identifiers: chr9:g.96929711del (hg19) ; chr9:g.94167429del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167432del , CM000671.2:g.94167432del	GRCh38
NC_000009.11:g.96929714del , CM000671.1:g.96929714del	GRCh37
NC_000009.10:g.95969535del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+1051del
NR_170275.1:n.124+1051del
NR_170276.1:n.124+1051del
NR_170277.1:n.124+1051del
NR_170278.1:n.124+1051del