Canonical Allele Identifier: CA89843836

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs147072881
• gnomAD v2: 3-185686798-T-TG
• gnomAD v3: 3-185969009-T-TG
• gnomAD v4: 3-185969009-T-TG
• MyVariant Identifiers: chr3:g.185686799_185686800insG (hg19) ; chr3:g.185686798_185686799insG (hg19) ; chr3:g.185969010_185969011insG (hg38) ; chr3:g.185969009_185969010insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185969017dup , CM000665.2:g.185969017dup	GRCh38
NC_000003.11:g.185686806dup , CM000665.1:g.185686806dup	GRCh37
NC_000003.10:g.187169500dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+309dup
ENST00000416764.5:n.349+300dup
ENST00000422108.5:n.288+368dup
ENST00000423298.5:n.137-2598dup
ENST00000436375.5:n.342+309dup
ENST00000445507.1:n.279+368dup
NR_033752.2:n.349+300dup
NR_151491.1:n.137-2598dup