Canonical Allele Identifier: CA1426720656
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969033C= , CM000665.2:g.185969033C= GRCh38
NC_000003.11:g.185686822C= , CM000665.1:g.185686822C= GRCh37
NC_000003.10:g.187169516C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+325C=
ENST00000416764.5:n.349+316C=
ENST00000422108.5:n.288+384C=
ENST00000423298.5:n.137-2582C=
ENST00000436375.5:n.342+325C=
ENST00000445507.1:n.279+384C=
NR_033752.2:n.349+316C=
NR_151491.1:n.137-2582C=