Canonical Allele Identifier: CA345689

Linked Data

ClinVar Variation Id: 96747
ClinVar RCV Id: RCV000128484
dbSNP Id: rs431825168

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2001029C>A , CM000673.2:g.2001029C>A GRCh38
NC_000011.9:g.2022259C>A , CM000673.1:g.2022259C>A GRCh37
NC_000011.8:g.1978835C>A NCBI36
NG_016165.1:g.1807G>T

Transcript Alleles

HGVS Amino-acid Change
NR_131224.1:n.249+189G>T (H19)
XM_011520273.1:c.498-10512C>A (MRPL23) XP_011518575.1:n.498-10512C>A
XM_011520274.1:c.492-10512C>A (MRPL23) XP_011518576.1:n.492-10512C>A
XM_011520275.1:c.498-10512C>A (MRPL23) XP_011518577.1:n.498-10512C>A
XM_011520275.2:c.498-10512C>A (MRPL23) XP_011518577.1:n.498-10512C>A
NM_001400176.1:c.498-10512C>A (MRPL23) NP_001387105.1:n.498-10512C>A