Canonical Allele Identifier: CA89843867
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs868331767
MyVariant Identifiers: chr3:g.185687007G>C (hg19) chr3:g.185969218G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969218G>C , CM000665.2:g.185969218G>C GRCh38
NC_000003.11:g.185687007G>C , CM000665.1:g.185687007G>C GRCh37
NC_000003.10:g.187169701G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+510G>C
ENST00000416764.5:n.349+501G>C
ENST00000422108.5:n.288+569G>C
ENST00000423298.5:n.137-2397G>C
ENST00000436375.5:n.342+510G>C
ENST00000445507.1:n.279+569G>C
NR_033752.2:n.349+501G>C
NR_151491.1:n.137-2397G>C
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