Canonical Allele Identifier: CA1426720529
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968942C= , CM000665.2:g.185968942C= GRCh38
NC_000003.11:g.185686731C= , CM000665.1:g.185686731C= GRCh37
NC_000003.10:g.187169425C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+234C=
ENST00000416764.5:n.349+225C=
ENST00000422108.5:n.288+293C=
ENST00000423298.5:n.137-2673C=
ENST00000436375.5:n.342+234C=
ENST00000445507.1:n.279+293C=
NR_033752.2:n.349+225C=
NR_151491.1:n.137-2673C=