Canonical Allele Identifier: CA903889238
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs1354363512

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968869_185968872del , CM000665.2:g.185968869_185968872del GRCh38
NC_000003.11:g.185686658_185686661del , CM000665.1:g.185686658_185686661del GRCh37
NC_000003.10:g.187169352_187169355del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+161_270+164del
ENST00000416764.5:n.349+152_349+155del
ENST00000422108.5:n.288+220_288+223del
ENST00000423298.5:n.137-2746_137-2743del
ENST00000436375.5:n.342+161_342+164del
ENST00000445507.1:n.279+220_279+223del
NR_033752.2:n.349+152_349+155del
NR_151491.1:n.137-2746_137-2743del