HGVS | Genome Assembly |
---|---|
NC_000011.10:g.1999156T>G , CM000673.2:g.1999156T>G | GRCh38 |
NC_000011.9:g.2020386T>G , CM000673.1:g.2020386T>G | GRCh37 |
NC_000011.8:g.1976962T>G | NCBI36 |
NG_016165.1:g.3680A>C |
HGVS | Amino-acid Change | |
---|---|---|
NR_131224.1:n.249+2062A>C (H19) | ||
XM_011520273.1:c.498-12385T>G (MRPL23) | XP_011518575.1:n.498-12385T>G | |
XM_011520274.1:c.492-12385T>G (MRPL23) | XP_011518576.1:n.492-12385T>G | |
XM_011520275.1:c.498-12385T>G (MRPL23) | XP_011518577.1:n.498-12385T>G | |
XM_011520275.2:c.498-12385T>G (MRPL23) | XP_011518577.1:n.498-12385T>G | |
NM_001400176.1:c.498-12385T>G (MRPL23) | NP_001387105.1:n.498-12385T>G |