Canonical Allele Identifier: CA89843869
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs977588163
MyVariant Identifiers: chr3:g.185687015G>A (hg19) chr3:g.185969226G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969226G>A , CM000665.2:g.185969226G>A GRCh38
NC_000003.11:g.185687015G>A , CM000665.1:g.185687015G>A GRCh37
NC_000003.10:g.187169709G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+518G>A
ENST00000416764.5:n.349+509G>A
ENST00000422108.5:n.288+577G>A
ENST00000423298.5:n.137-2389G>A
ENST00000436375.5:n.342+518G>A
ENST00000445507.1:n.279+577G>A
NR_033752.2:n.349+509G>A
NR_151491.1:n.137-2389G>A
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