Canonical Allele Identifier: CA903889517
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs1217371271
MyVariant Identifiers: chr3:g.185687096C>A (hg19) chr3:g.185969307C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969307C>A , CM000665.2:g.185969307C>A GRCh38
NC_000003.11:g.185687096C>A , CM000665.1:g.185687096C>A GRCh37
NC_000003.10:g.187169790C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+599C>A
ENST00000416764.5:n.349+590C>A
ENST00000422108.5:n.288+658C>A
ENST00000423298.5:n.137-2308C>A
ENST00000436375.5:n.342+599C>A
ENST00000445507.1:n.279+658C>A
NR_033752.2:n.349+590C>A
NR_151491.1:n.137-2308C>A
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