Canonical Allele Identifier: CA89843876
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs954086679
MyVariant Identifiers: chr3:g.185687056G>T (hg19) chr3:g.185969267G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969267G>T , CM000665.2:g.185969267G>T GRCh38
NC_000003.11:g.185687056G>T , CM000665.1:g.185687056G>T GRCh37
NC_000003.10:g.187169750G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+559G>T
ENST00000416764.5:n.349+550G>T
ENST00000422108.5:n.288+618G>T
ENST00000423298.5:n.137-2348G>T
ENST00000436375.5:n.342+559G>T
ENST00000445507.1:n.279+618G>T
NR_033752.2:n.349+550G>T
NR_151491.1:n.137-2348G>T
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