Canonical Allele Identifier: CA2668921131
Gene: NMRAL2P HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968802A>G , CM000665.2:g.185968802A>G GRCh38
NC_000003.11:g.185686591A>G , CM000665.1:g.185686591A>G GRCh37
NC_000003.10:g.187169285A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+94A>G
ENST00000416764.5:n.349+85A>G
ENST00000422108.5:n.288+153A>G
ENST00000423298.5:n.137-2813A>G
ENST00000436375.5:n.342+94A>G
ENST00000445507.1:n.279+153A>G
NR_033752.2:n.349+85A>G
NR_151491.1:n.137-2813A>G