Canonical Allele Identifier: CA346914
Gene: MRPL23 HGNC NCBI

Linked Data

ClinVar Variation Id: 156466
ClinVar RCV Id: RCV000190278
dbSNP Id: rs587777745
MyVariant Identifiers: chr11:g.2022993T>G (hg19) chr11:g.2001763T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2001763T>G , CM000673.2:g.2001763T>G GRCh38
NC_000011.9:g.2022993T>G , CM000673.1:g.2022993T>G GRCh37
NC_000011.8:g.1979569T>G NCBI36
NG_016165.1:g.1073A>C

Transcript Alleles

HGVS Amino-acid Change
XM_011520273.1:c.498-9778T>G XP_011518575.1:n.498-9778T>G
XM_011520274.1:c.492-9778T>G XP_011518576.1:n.492-9778T>G
XM_011520275.1:c.498-9778T>G XP_011518577.1:n.498-9778T>G
XM_011520275.2:c.498-9778T>G XP_011518577.1:n.498-9778T>G
NM_001400176.1:c.498-9778T>G NP_001387105.1:n.498-9778T>G
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