HGVS | Genome Assembly |
---|---|
NC_000009.12:g.127814182A= , CM000671.2:g.127814182A= | GRCh38 |
NC_000009.11:g.130576461A= , CM000671.1:g.130576461A= | GRCh37 |
NC_000009.10:g.129616282A= | NCBI36 |
NG_009551.1:g.45587T= , LRG_589:g.45587T= | |
NG_023245.1:g.16308A= |
HGVS | Amino-acid Change |
---|---|
ENST00000467826.5:n.710-26A= | |
XM_005251864.2:c.1484-26A= | XP_005251921.1:n.1484-26A= |
XM_005251864.4:c.1484-26A= | XP_005251921.1:n.1484-26A= |
XM_017014565.2:c.1334-26A= | XP_016870054.1:n.1334-26A= |
XR_242582.2:n.1381-26A= | |
XR_242582.4:n.1379-26A= |