Canonical Allele Identifier: CA5817502

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1996938C>T , CM000673.2:g.1996938C>T GRCh38
NC_000011.9:g.2018168C>T , CM000673.1:g.2018168C>T GRCh37
NC_000011.8:g.1974744C>T NCBI36
NG_016165.1:g.5898G>A
NG_045220.1:g.9531C>T

Transcript Alleles

HGVS Amino-acid Change
NR_002196.2:n.938G>A (H19)
NR_131223.1:n.938G>A (H19)
NR_131224.1:n.250-517G>A (H19)
XM_011520273.1:c.498-14603C>T (MRPL23) XP_011518575.1:n.498-14603C>T
XM_011520274.1:c.492-14603C>T (MRPL23) XP_011518576.1:n.492-14603C>T
XM_011520275.1:c.498-14603C>T (MRPL23) XP_011518577.1:n.498-14603C>T
XM_011520275.2:c.498-14603C>T (MRPL23) XP_011518577.1:n.498-14603C>T
NM_001400176.1:c.498-14603C>T (MRPL23) NP_001387105.1:n.498-14603C>T