Canonical Allele Identifier: CA1426720877
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969296A= , CM000665.2:g.185969296A= GRCh38
NC_000003.11:g.185687085A= , CM000665.1:g.185687085A= GRCh37
NC_000003.10:g.187169779A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+588A=
ENST00000416764.5:n.349+579A=
ENST00000422108.5:n.288+647A=
ENST00000423298.5:n.137-2319A=
ENST00000436375.5:n.342+588A=
ENST00000445507.1:n.279+647A=
NR_033752.2:n.349+579A=
NR_151491.1:n.137-2319A=