Canonical Allele Identifier: CA269951
Gene: MRPL23 HGNC NCBI

Linked Data

ClinVar Variation Id: 96742
ClinVar RCV Id: RCV000128479
dbSNP Id: rs431825163
MyVariant Identifiers: chr11:g.2023045G>A (hg19) chr11:g.2001815G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2001815G>A , CM000673.2:g.2001815G>A GRCh38
NC_000011.9:g.2023045G>A , CM000673.1:g.2023045G>A GRCh37
NC_000011.8:g.1979621G>A NCBI36
NG_016165.1:g.1021C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520273.1:c.498-9726G>A XP_011518575.1:n.498-9726G>A
XM_011520274.1:c.492-9726G>A XP_011518576.1:n.492-9726G>A
XM_011520275.1:c.498-9726G>A XP_011518577.1:n.498-9726G>A
XM_011520275.2:c.498-9726G>A XP_011518577.1:n.498-9726G>A
NM_001400176.1:c.498-9726G>A NP_001387105.1:n.498-9726G>A
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