Canonical Allele Identifier: CA89843835
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs921523413
gnomAD v3: 3-185969002-C-T
gnomAD v4: 3-185969002-C-T
MyVariant Identifiers: chr3:g.185686791C>T (hg19) chr3:g.185969002C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969002C>T , CM000665.2:g.185969002C>T GRCh38
NC_000003.11:g.185686791C>T , CM000665.1:g.185686791C>T GRCh37
NC_000003.10:g.187169485C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+294C>T
ENST00000416764.5:n.349+285C>T
ENST00000422108.5:n.288+353C>T
ENST00000423298.5:n.137-2613C>T
ENST00000436375.5:n.342+294C>T
ENST00000445507.1:n.279+353C>T
NR_033752.2:n.349+285C>T
NR_151491.1:n.137-2613C>T
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