Canonical Allele Identifier: CA1426720854
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969284C= , CM000665.2:g.185969284C= GRCh38
NC_000003.11:g.185687073C= , CM000665.1:g.185687073C= GRCh37
NC_000003.10:g.187169767C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+576C=
ENST00000416764.5:n.349+567C=
ENST00000422108.5:n.288+635C=
ENST00000423298.5:n.137-2331C=
ENST00000436375.5:n.342+576C=
ENST00000445507.1:n.279+635C=
NR_033752.2:n.349+567C=
NR_151491.1:n.137-2331C=