Canonical Allele Identifier: CA903889451
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs1378981445
gnomAD v3: 3-185969151-C-G
gnomAD v4: 3-185969151-C-G
MyVariant Identifiers: chr3:g.185686940C>G (hg19) chr3:g.185969151C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969151C>G , CM000665.2:g.185969151C>G GRCh38
NC_000003.11:g.185686940C>G , CM000665.1:g.185686940C>G GRCh37
NC_000003.10:g.187169634C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+443C>G
ENST00000416764.5:n.349+434C>G
ENST00000422108.5:n.288+502C>G
ENST00000423298.5:n.137-2464C>G
ENST00000436375.5:n.342+443C>G
ENST00000445507.1:n.279+502C>G
NR_033752.2:n.349+434C>G
NR_151491.1:n.137-2464C>G
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