Canonical Allele Identifier: CA2668921174
Gene: NMRAL2P HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968861G>A , CM000665.2:g.185968861G>A GRCh38
NC_000003.11:g.185686650G>A , CM000665.1:g.185686650G>A GRCh37
NC_000003.10:g.187169344G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306399.3:n.270+153G>A
ENST00000416764.5:n.349+144G>A
ENST00000422108.5:n.288+212G>A
ENST00000423298.5:n.137-2754G>A
ENST00000436375.5:n.342+153G>A
ENST00000445507.1:n.279+212G>A
NR_033752.2:n.349+144G>A
NR_151491.1:n.137-2754G>A