Canonical Allele Identifier: CA2668921092
Gene: NMRAL2P HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968763T>C , CM000665.2:g.185968763T>C GRCh38
NC_000003.11:g.185686552T>C , CM000665.1:g.185686552T>C GRCh37
NC_000003.10:g.187169246T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+55T>C
ENST00000416764.5:n.349+46T>C
ENST00000422108.5:n.288+114T>C
ENST00000423298.5:n.137-2852T>C
ENST00000436375.5:n.342+55T>C
ENST00000445507.1:n.279+114T>C
NR_033752.2:n.349+46T>C
NR_151491.1:n.137-2852T>C