Canonical Allele Identifier: CA903889313
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs1479016848

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968945_185968946del , CM000665.2:g.185968945_185968946del GRCh38
NC_000003.11:g.185686734_185686735del , CM000665.1:g.185686734_185686735del GRCh37
NC_000003.10:g.187169428_187169429del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+237_270+238del
ENST00000416764.5:n.349+228_349+229del
ENST00000422108.5:n.288+296_288+297del
ENST00000423298.5:n.137-2670_137-2669del
ENST00000436375.5:n.342+237_342+238del
ENST00000445507.1:n.279+296_279+297del
NR_033752.2:n.349+228_349+229del
NR_151491.1:n.137-2670_137-2669del