Canonical Allele Identifier: CA216219933

Linked Data

dbSNP Id: rs1013167425
MyVariant Identifiers: chr11:g.1999378A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999378A>C , CM000673.2:g.1999378A>C GRCh38
NC_000011.9:g.2020608A>C , CM000673.1:g.2020608A>C GRCh37
NC_000011.8:g.1977184A>C NCBI36
NG_016165.1:g.3458T>G

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1840T>G (H19)
XM_011520273.1:c.498-12163A>C (MRPL23) XP_011518575.1:n.498-12163A>C
XM_011520274.1:c.492-12163A>C (MRPL23) XP_011518576.1:n.492-12163A>C
XM_011520275.1:c.498-12163A>C (MRPL23) XP_011518577.1:n.498-12163A>C
XM_011520275.2:c.498-12163A>C (MRPL23) XP_011518577.1:n.498-12163A>C
NM_001400176.1:c.498-12163A>C (MRPL23) NP_001387105.1:n.498-12163A>C