Canonical Allele Identifier: CA597072524

Linked Data

gnomAD v2: 11-2020577-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999347G>A , CM000673.2:g.1999347G>A GRCh38
NC_000011.9:g.2020577G>A , CM000673.1:g.2020577G>A GRCh37
NC_000011.8:g.1977153G>A NCBI36
NG_016165.1:g.3489C>T

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1871C>T (H19)
XM_011520273.1:c.498-12194G>A (MRPL23) XP_011518575.1:n.498-12194G>A
XM_011520274.1:c.492-12194G>A (MRPL23) XP_011518576.1:n.492-12194G>A
XM_011520275.1:c.498-12194G>A (MRPL23) XP_011518577.1:n.498-12194G>A
XM_011520275.2:c.498-12194G>A (MRPL23) XP_011518577.1:n.498-12194G>A
NM_001400176.1:c.498-12194G>A (MRPL23) NP_001387105.1:n.498-12194G>A