Canonical Allele Identifier: CA1057368981
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs1744963982
gnomAD v3: 3-185968943-A-G
gnomAD v4: 3-185968943-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968943A>G , CM000665.2:g.185968943A>G GRCh38
NC_000003.11:g.185686732A>G , CM000665.1:g.185686732A>G GRCh37
NC_000003.10:g.187169426A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+235A>G
ENST00000416764.5:n.349+226A>G
ENST00000422108.5:n.288+294A>G
ENST00000423298.5:n.137-2672A>G
ENST00000436375.5:n.342+235A>G
ENST00000445507.1:n.279+294A>G
NR_033752.2:n.349+226A>G
NR_151491.1:n.137-2672A>G
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