Canonical Allele Identifier: CA1057368995
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs1744967726
gnomAD v3: 3-185969210-G-A
gnomAD v4: 3-185969210-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969210G>A , CM000665.2:g.185969210G>A GRCh38
NC_000003.11:g.185686999G>A , CM000665.1:g.185686999G>A GRCh37
NC_000003.10:g.187169693G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+502G>A
ENST00000416764.5:n.349+493G>A
ENST00000422108.5:n.288+561G>A
ENST00000423298.5:n.137-2405G>A
ENST00000436375.5:n.342+502G>A
ENST00000445507.1:n.279+561G>A
NR_033752.2:n.349+493G>A
NR_151491.1:n.137-2405G>A
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