Canonical Allele Identifier: CA1947947914

Linked Data

dbSNP Id: rs1857063113

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999864_1999865del , CM000673.2:g.1999864_1999865del GRCh38
NC_000011.9:g.2021094_2021095del , CM000673.1:g.2021094_2021095del GRCh37
NC_000011.8:g.1977670_1977671del NCBI36
NG_016165.1:g.2972_2973del

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1354_249+1355del (H19)
XM_011520273.1:c.498-11677_498-11676del (MRPL23) XP_011518575.1:n.498-11677_498-11676del
XM_011520274.1:c.492-11677_492-11676del (MRPL23) XP_011518576.1:n.492-11677_492-11676del
XM_011520275.1:c.498-11677_498-11676del (MRPL23) XP_011518577.1:n.498-11677_498-11676del
XM_011520275.2:c.498-11677_498-11676del (MRPL23) XP_011518577.1:n.498-11677_498-11676del
NM_001400176.1:c.498-11677_498-11676del (MRPL23) NP_001387105.1:n.498-11677_498-11676del