HGVS | Genome Assembly |
---|---|
NC_000011.10:g.1999788T>C , CM000673.2:g.1999788T>C | GRCh38 |
NC_000011.9:g.2021018T>C , CM000673.1:g.2021018T>C | GRCh37 |
NC_000011.8:g.1977594T>C | NCBI36 |
NG_016165.1:g.3048A>G |
HGVS | Amino-acid Change | |
---|---|---|
NR_131224.1:n.249+1430A>G (H19) | ||
XM_011520273.1:c.498-11753T>C (MRPL23) | XP_011518575.1:n.498-11753T>C | |
XM_011520274.1:c.492-11753T>C (MRPL23) | XP_011518576.1:n.492-11753T>C | |
XM_011520275.1:c.498-11753T>C (MRPL23) | XP_011518577.1:n.498-11753T>C | |
XM_011520275.2:c.498-11753T>C (MRPL23) | XP_011518577.1:n.498-11753T>C | |
NM_001400176.1:c.498-11753T>C (MRPL23) | NP_001387105.1:n.498-11753T>C |