Canonical Allele Identifier: CA1426720828
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969258G= , CM000665.2:g.185969258G= GRCh38
NC_000003.11:g.185687047G= , CM000665.1:g.185687047G= GRCh37
NC_000003.10:g.187169741G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+550G=
ENST00000416764.5:n.349+541G=
ENST00000422108.5:n.288+609G=
ENST00000423298.5:n.137-2357G=
ENST00000436375.5:n.342+550G=
ENST00000445507.1:n.279+609G=
NR_033752.2:n.349+541G=
NR_151491.1:n.137-2357G=