Canonical Allele Identifier: CA89843865
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs192118973
gnomAD v2: 3-185686991-A-T
gnomAD v3: 3-185969202-A-T
gnomAD v4: 3-185969202-A-T
MyVariant Identifiers: chr3:g.185686991A>T (hg19) chr3:g.185969202A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969202A>T , CM000665.2:g.185969202A>T GRCh38
NC_000003.11:g.185686991A>T , CM000665.1:g.185686991A>T GRCh37
NC_000003.10:g.187169685A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+494A>T
ENST00000416764.5:n.349+485A>T
ENST00000422108.5:n.288+553A>T
ENST00000423298.5:n.137-2413A>T
ENST00000436375.5:n.342+494A>T
ENST00000445507.1:n.279+553A>T
NR_033752.2:n.349+485A>T
NR_151491.1:n.137-2413A>T
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