Canonical Allele Identifier: CA548616985

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs147072881
• gnomAD v2: 3-185686798-T-TGG
• gnomAD v3: 3-185969009-T-TGG
• gnomAD v4: 3-185969009-T-TGG
• MyVariant Identifiers: chr3:g.185686799_185686800insGG (hg19) ; chr3:g.185686798_185686799insGG (hg19) ; chr3:g.185969010_185969011insGG (hg38) ; chr3:g.185969009_185969010insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185969016_185969017dup , CM000665.2:g.185969016_185969017dup	GRCh38
NC_000003.11:g.185686805_185686806dup , CM000665.1:g.185686805_185686806dup	GRCh37
NC_000003.10:g.187169499_187169500dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+308_270+309dup
ENST00000416764.5:n.349+299_349+300dup
ENST00000422108.5:n.288+367_288+368dup
ENST00000423298.5:n.137-2599_137-2598dup
ENST00000436375.5:n.342+308_342+309dup
ENST00000445507.1:n.279+367_279+368dup
NR_033752.2:n.349+299_349+300dup
NR_151491.1:n.137-2599_137-2598dup