Canonical Allele Identifier: CA1426720888
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs185048638

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969301C>G , CM000665.2:g.185969301C>G GRCh38
NC_000003.11:g.185687090C>G , CM000665.1:g.185687090C>G GRCh37
NC_000003.10:g.187169784C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+593C>G
ENST00000416764.5:n.349+584C>G
ENST00000422108.5:n.288+652C>G
ENST00000423298.5:n.137-2314C>G
ENST00000436375.5:n.342+593C>G
ENST00000445507.1:n.279+652C>G
NR_033752.2:n.349+584C>G
NR_151491.1:n.137-2314C>G