Canonical Allele Identifier: CA597072871

Linked Data

dbSNP Id: rs1208171842
gnomAD v2: 11-2021128-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999898G>C , CM000673.2:g.1999898G>C GRCh38
NC_000011.9:g.2021128G>C , CM000673.1:g.2021128G>C GRCh37
NC_000011.8:g.1977704G>C NCBI36
NG_016165.1:g.2938C>G

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1320C>G (H19)
XM_011520273.1:c.498-11643G>C (MRPL23) XP_011518575.1:n.498-11643G>C
XM_011520274.1:c.492-11643G>C (MRPL23) XP_011518576.1:n.492-11643G>C
XM_011520275.1:c.498-11643G>C (MRPL23) XP_011518577.1:n.498-11643G>C
XM_011520275.2:c.498-11643G>C (MRPL23) XP_011518577.1:n.498-11643G>C
NM_001400176.1:c.498-11643G>C (MRPL23) NP_001387105.1:n.498-11643G>C