Canonical Allele Identifier: CA1947947738

Linked Data

dbSNP Id: rs1857057868

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999322del , CM000673.2:g.1999322del GRCh38
NC_000011.9:g.2020552del , CM000673.1:g.2020552del GRCh37
NC_000011.8:g.1977128del NCBI36
NG_016165.1:g.3515del

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1897del (H19)
XM_011520273.1:c.498-12219del (MRPL23) XP_011518575.1:n.498-12219del
XM_011520274.1:c.492-12219del (MRPL23) XP_011518576.1:n.492-12219del
XM_011520275.1:c.498-12219del (MRPL23) XP_011518577.1:n.498-12219del
XM_011520275.2:c.498-12219del (MRPL23) XP_011518577.1:n.498-12219del
NM_001400176.1:c.498-12219del (MRPL23) NP_001387105.1:n.498-12219del