Canonical Allele Identifier: CA1426720753
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs1744967278

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969166T>C , CM000665.2:g.185969166T>C GRCh38
NC_000003.11:g.185686955T>C , CM000665.1:g.185686955T>C GRCh37
NC_000003.10:g.187169649T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+458T>C
ENST00000416764.5:n.349+449T>C
ENST00000422108.5:n.288+517T>C
ENST00000423298.5:n.137-2449T>C
ENST00000436375.5:n.342+458T>C
ENST00000445507.1:n.279+517T>C
NR_033752.2:n.349+449T>C
NR_151491.1:n.137-2449T>C