Canonical Allele Identifier: CA2668921108
Gene: NMRAL2P HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968772T>G , CM000665.2:g.185968772T>G GRCh38
NC_000003.11:g.185686561T>G , CM000665.1:g.185686561T>G GRCh37
NC_000003.10:g.187169255T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306399.3:n.270+64T>G
ENST00000416764.5:n.349+55T>G
ENST00000422108.5:n.288+123T>G
ENST00000423298.5:n.137-2843T>G
ENST00000436375.5:n.342+64T>G
ENST00000445507.1:n.279+123T>G
NR_033752.2:n.349+55T>G
NR_151491.1:n.137-2843T>G