Canonical Allele Identifier: CA1426720875

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs1334389287

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185969293G>C , CM000665.2:g.185969293G>C	GRCh38
NC_000003.11:g.185687082G>C , CM000665.1:g.185687082G>C	GRCh37
NC_000003.10:g.187169776G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+585G>C
ENST00000416764.5:n.349+576G>C
ENST00000422108.5:n.288+644G>C
ENST00000423298.5:n.137-2322G>C
ENST00000436375.5:n.342+585G>C
ENST00000445507.1:n.279+644G>C
NR_033752.2:n.349+576G>C
NR_151491.1:n.137-2322G>C