Canonical Allele Identifier: CA89843837

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs934262008
• gnomAD v2: 3-185686800-G-GC
• gnomAD v3: 3-185969011-G-GC
• gnomAD v4: 3-185969011-G-GC
• MyVariant Identifiers: chr3:g.185686800_185686801insC (hg19) ; chr3:g.185969011_185969012insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185969011_185969012insC , CM000665.2:g.185969011_185969012insC	GRCh38
NC_000003.11:g.185686800_185686801insC , CM000665.1:g.185686800_185686801insC	GRCh37
NC_000003.10:g.187169494_187169495insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+303_270+304insC
ENST00000416764.5:n.349+294_349+295insC
ENST00000422108.5:n.288+362_288+363insC
ENST00000423298.5:n.137-2604_137-2603insC
ENST00000436375.5:n.342+303_342+304insC
ENST00000445507.1:n.279+362_279+363insC
NR_033752.2:n.349+294_349+295insC
NR_151491.1:n.137-2604_137-2603insC