Canonical Allele Identifier: CA1426720849
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969277C= , CM000665.2:g.185969277C= GRCh38
NC_000003.11:g.185687066C= , CM000665.1:g.185687066C= GRCh37
NC_000003.10:g.187169760C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+569C=
ENST00000416764.5:n.349+560C=
ENST00000422108.5:n.288+628C=
ENST00000423298.5:n.137-2338C=
ENST00000436375.5:n.342+569C=
ENST00000445507.1:n.279+628C=
NR_033752.2:n.349+560C=
NR_151491.1:n.137-2338C=