Canonical Allele Identifier: CA2668921129
Gene: NMRAL2P HGNC NCBI

Linked Data

gnomAD v4: 3-185968797-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968797G>T , CM000665.2:g.185968797G>T GRCh38
NC_000003.11:g.185686586G>T , CM000665.1:g.185686586G>T GRCh37
NC_000003.10:g.187169280G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+89G>T
ENST00000416764.5:n.349+80G>T
ENST00000422108.5:n.288+148G>T
ENST00000423298.5:n.137-2818G>T
ENST00000436375.5:n.342+89G>T
ENST00000445507.1:n.279+148G>T
NR_033752.2:n.349+80G>T
NR_151491.1:n.137-2818G>T
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