Canonical Allele Identifier: CA1426720725
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs11715535

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969147A>T , CM000665.2:g.185969147A>T GRCh38
NC_000003.11:g.185686936A>T , CM000665.1:g.185686936A>T GRCh37
NC_000003.10:g.187169630A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+439A>T
ENST00000416764.5:n.349+430A>T
ENST00000422108.5:n.288+498A>T
ENST00000423298.5:n.137-2468A>T
ENST00000436375.5:n.342+439A>T
ENST00000445507.1:n.279+498A>T
NR_033752.2:n.349+430A>T
NR_151491.1:n.137-2468A>T