Canonical Allele Identifier: CA1947947912

Linked Data

dbSNP Id: rs1857063070

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999861_1999862insT , CM000673.2:g.1999861_1999862insT GRCh38
NC_000011.9:g.2021091_2021092insT , CM000673.1:g.2021091_2021092insT GRCh37
NC_000011.8:g.1977667_1977668insT NCBI36
NG_016165.1:g.2974_2975insA

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1356_249+1357insA (H19)
XM_011520273.1:c.498-11680_498-11679insT (MRPL23) XP_011518575.1:n.498-11680_498-11679insT
XM_011520274.1:c.492-11680_492-11679insT (MRPL23) XP_011518576.1:n.492-11680_492-11679insT
XM_011520275.1:c.498-11680_498-11679insT (MRPL23) XP_011518577.1:n.498-11680_498-11679insT
XM_011520275.2:c.498-11680_498-11679insT (MRPL23) XP_011518577.1:n.498-11680_498-11679insT
NM_001400176.1:c.498-11680_498-11679insT (MRPL23) NP_001387105.1:n.498-11680_498-11679insT