Canonical Allele Identifier: CA2668921111
Gene: NMRAL2P HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968774G>T , CM000665.2:g.185968774G>T GRCh38
NC_000003.11:g.185686563G>T , CM000665.1:g.185686563G>T GRCh37
NC_000003.10:g.187169257G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+66G>T
ENST00000416764.5:n.349+57G>T
ENST00000422108.5:n.288+125G>T
ENST00000423298.5:n.137-2841G>T
ENST00000436375.5:n.342+66G>T
ENST00000445507.1:n.279+125G>T
NR_033752.2:n.349+57G>T
NR_151491.1:n.137-2841G>T