Canonical Allele Identifier: CA548616986

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs1421770063
• gnomAD v2: 3-185686799-G-GT
• gnomAD v3: 3-185969010-G-GT
• gnomAD v4: 3-185969010-G-GT
• MyVariant Identifiers: chr3:g.185686799_185686800insT (hg19) ; chr3:g.185969010_185969011insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185969010_185969011insT , CM000665.2:g.185969010_185969011insT	GRCh38
NC_000003.11:g.185686799_185686800insT , CM000665.1:g.185686799_185686800insT	GRCh37
NC_000003.10:g.187169493_187169494insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+302_270+303insT
ENST00000416764.5:n.349+293_349+294insT
ENST00000422108.5:n.288+361_288+362insT
ENST00000423298.5:n.137-2605_137-2604insT
ENST00000436375.5:n.342+302_342+303insT
ENST00000445507.1:n.279+361_279+362insT
NR_033752.2:n.349+293_349+294insT
NR_151491.1:n.137-2605_137-2604insT