Canonical Allele Identifier: CA1426720461
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968872A= , CM000665.2:g.185968872A= GRCh38
NC_000003.11:g.185686661A= , CM000665.1:g.185686661A= GRCh37
NC_000003.10:g.187169355A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306399.3:n.270+164A=
ENST00000416764.5:n.349+155A=
ENST00000422108.5:n.288+223A=
ENST00000423298.5:n.137-2743A=
ENST00000436375.5:n.342+164A=
ENST00000445507.1:n.279+223A=
NR_033752.2:n.349+155A=
NR_151491.1:n.137-2743A=