Canonical Allele Identifier: CA89843883
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs570902351
MyVariant Identifiers: chr3:g.185687101T>C (hg19) chr3:g.185969312T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969312T>C , CM000665.2:g.185969312T>C GRCh38
NC_000003.11:g.185687101T>C , CM000665.1:g.185687101T>C GRCh37
NC_000003.10:g.187169795T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+604T>C
ENST00000416764.5:n.349+595T>C
ENST00000422108.5:n.288+663T>C
ENST00000423298.5:n.137-2303T>C
ENST00000436375.5:n.342+604T>C
ENST00000445507.1:n.279+663T>C
NR_033752.2:n.349+595T>C
NR_151491.1:n.137-2303T>C
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