Canonical Allele Identifier: CA216219885

Linked Data

MyVariant Identifiers: chr11:g.1999359C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999359C>T , CM000673.2:g.1999359C>T GRCh38
NC_000011.9:g.2020589C>T , CM000673.1:g.2020589C>T GRCh37
NC_000011.8:g.1977165C>T NCBI36
NG_016165.1:g.3477G>A

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1859G>A (H19)
XM_011520273.1:c.498-12182C>T (MRPL23) XP_011518575.1:n.498-12182C>T
XM_011520274.1:c.492-12182C>T (MRPL23) XP_011518576.1:n.492-12182C>T
XM_011520275.1:c.498-12182C>T (MRPL23) XP_011518577.1:n.498-12182C>T
XM_011520275.2:c.498-12182C>T (MRPL23) XP_011518577.1:n.498-12182C>T
NM_001400176.1:c.498-12182C>T (MRPL23) NP_001387105.1:n.498-12182C>T