HGVS | Genome Assembly |
---|---|
NC_000017.11:g.12019847A>T , CM000679.2:g.12019847A>T | GRCh38 |
NC_000017.10:g.11923164A>T , CM000679.1:g.11923164A>T | GRCh37 |
NC_000017.9:g.11863889A>T | NCBI36 |
NG_033952.1:g.4030A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000578024.1:n.24+1476T>A (RPL21P122) | ||
ENST00000579522.1:n.186+1476T>A (RPL21P122) | ||
XR_934231.1:n.143+733T>A | ||
XM_024450911.1:c.-329+1476T>A (ZNF18) | XP_024306679.1:n.-329+1476T>A |