Canonical Allele Identifier: CA9946555
Gene: MIR1-1HG HGNC NCBI
MIR1-1 HGNC NCBI
MyVariant.info:
GRCh38 chr20:g.62554308G>A
GRCh37 chr20:g.61151515G>A
gnomAD v2:
20:61151515 G / A
gnomAD v3:
20:62554308 G / A
gnomAD v4:
chr20-62554308-G-A
Joint Max Group AF 0.01908711 (AFR)
Genomes Max Group AF 0.01907443 (AFR)
Exomes Max Group AF 0.01744885 (AFR)
dbSNP:
6122014
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62554308G>A , CM000682.2:g.62554308G>A GRCh38
NC_000020.10:g.61151515G>A , CM000682.1:g.61151515G>A GRCh37
NC_000020.9:g.60561960G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001302812.1:c.8+643G>A (MIR1-1HG) NP_001289741.1:n.8+643G>A
NM_178463.3:c.8+643G>A (MIR1-1HG) NP_848558.1:n.8+643G>A
NR_029780.1:n.3G>A (MIR1-1)
NM_001302812.2:c.8+643G>A (MIR1-1HG) NP_001289741.1:n.8+643G>A
NM_178463.4:c.8+643G>A (MIR1-1HG) NP_848558.1:n.8+643G>A
NR_171007.1:n.787+643G>A (MIR1-1HG)
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