Canonical Allele Identifier: CA1426720641
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969017G= , CM000665.2:g.185969017G= GRCh38
NC_000003.11:g.185686806G= , CM000665.1:g.185686806G= GRCh37
NC_000003.10:g.187169500G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+309G=
ENST00000416764.5:n.349+300G=
ENST00000422108.5:n.288+368G=
ENST00000423298.5:n.137-2598G=
ENST00000436375.5:n.342+309G=
ENST00000445507.1:n.279+368G=
NR_033752.2:n.349+300G=
NR_151491.1:n.137-2598G=