Canonical Allele Identifier: CA903889487
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs1180373631

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969280_185969283del , CM000665.2:g.185969280_185969283del GRCh38
NC_000003.11:g.185687069_185687072del , CM000665.1:g.185687069_185687072del GRCh37
NC_000003.10:g.187169763_187169766del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+572_270+575del
ENST00000416764.5:n.349+563_349+566del
ENST00000422108.5:n.288+631_288+634del
ENST00000423298.5:n.137-2335_137-2332del
ENST00000436375.5:n.342+572_342+575del
ENST00000445507.1:n.279+631_279+634del
NR_033752.2:n.349+563_349+566del
NR_151491.1:n.137-2335_137-2332del