Canonical Allele Identifier: CA589477080

Gene: MIRLET7A1HG

Linked Data

• dbSNP Id: rs1370369393
• gnomAD v2: 9-96929299-CCCTT-C
• gnomAD v3: 9-94167017-CCCTT-C
• gnomAD v4: 9-94167017-CCCTT-C
• MyVariant Identifiers: chr9:g.96929300_96929303del (hg19) ; chr9:g.94167018_94167021del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94167021_94167024del , CM000671.2:g.94167021_94167024del	GRCh38
NC_000009.11:g.96929303_96929306del , CM000671.1:g.96929303_96929306del	GRCh37
NC_000009.10:g.95969124_95969127del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_170274.1:n.124+640_124+643del
NR_170275.1:n.124+640_124+643del
NR_170276.1:n.124+640_124+643del
NR_170277.1:n.124+640_124+643del
NR_170278.1:n.124+640_124+643del