Canonical Allele Identifier: CA1947947778

Linked Data

dbSNP Id: rs1857058786

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999380C>A , CM000673.2:g.1999380C>A GRCh38
NC_000011.9:g.2020610C>A , CM000673.1:g.2020610C>A GRCh37
NC_000011.8:g.1977186C>A NCBI36
NG_016165.1:g.3456G>T

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1838G>T (H19)
XM_011520273.1:c.498-12161C>A (MRPL23) XP_011518575.1:n.498-12161C>A
XM_011520274.1:c.492-12161C>A (MRPL23) XP_011518576.1:n.492-12161C>A
XM_011520275.1:c.498-12161C>A (MRPL23) XP_011518577.1:n.498-12161C>A
XM_011520275.2:c.498-12161C>A (MRPL23) XP_011518577.1:n.498-12161C>A
NM_001400176.1:c.498-12161C>A (MRPL23) NP_001387105.1:n.498-12161C>A