Canonical Allele Identifier: CA1426720377
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs1744961396

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968769C>T , CM000665.2:g.185968769C>T GRCh38
NC_000003.11:g.185686558C>T , CM000665.1:g.185686558C>T GRCh37
NC_000003.10:g.187169252C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306399.3:n.270+61C>T
ENST00000416764.5:n.349+52C>T
ENST00000422108.5:n.288+120C>T
ENST00000423298.5:n.137-2846C>T
ENST00000436375.5:n.342+61C>T
ENST00000445507.1:n.279+120C>T
NR_033752.2:n.349+52C>T
NR_151491.1:n.137-2846C>T