Canonical Allele Identifier: CA1426720645
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969018T= , CM000665.2:g.185969018T= GRCh38
NC_000003.11:g.185686807T= , CM000665.1:g.185686807T= GRCh37
NC_000003.10:g.187169501T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+310T=
ENST00000416764.5:n.349+301T=
ENST00000422108.5:n.288+369T=
ENST00000423298.5:n.137-2597T=
ENST00000436375.5:n.342+310T=
ENST00000445507.1:n.279+369T=
NR_033752.2:n.349+301T=
NR_151491.1:n.137-2597T=