Canonical Allele Identifier: CA2668921167
Gene: NMRAL2P HGNC NCBI

Linked Data

gnomAD v4: 3-185968850-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968850A>G , CM000665.2:g.185968850A>G GRCh38
NC_000003.11:g.185686639A>G , CM000665.1:g.185686639A>G GRCh37
NC_000003.10:g.187169333A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+142A>G
ENST00000416764.5:n.349+133A>G
ENST00000422108.5:n.288+201A>G
ENST00000423298.5:n.137-2765A>G
ENST00000436375.5:n.342+142A>G
ENST00000445507.1:n.279+201A>G
NR_033752.2:n.349+133A>G
NR_151491.1:n.137-2765A>G
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