Canonical Allele Identifier: CA2723166789

Linked Data

dbSNP Id: rs2119654176

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999830A>G , CM000673.2:g.1999830A>G GRCh38
NC_000011.9:g.2021060A>G , CM000673.1:g.2021060A>G GRCh37
NC_000011.8:g.1977636A>G NCBI36
NG_016165.1:g.3006T>C

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1388T>C (H19)
XM_011520273.1:c.498-11711A>G (MRPL23) XP_011518575.1:n.498-11711A>G
XM_011520274.1:c.492-11711A>G (MRPL23) XP_011518576.1:n.492-11711A>G
XM_011520275.1:c.498-11711A>G (MRPL23) XP_011518577.1:n.498-11711A>G
XM_011520275.2:c.498-11711A>G (MRPL23) XP_011518577.1:n.498-11711A>G
NM_001400176.1:c.498-11711A>G (MRPL23) NP_001387105.1:n.498-11711A>G