HGVS | Genome Assembly |
---|---|
NC_000009.12:g.127814184T>G , CM000671.2:g.127814184T>G | GRCh38 |
NC_000009.11:g.130576463T>G , CM000671.1:g.130576463T>G | GRCh37 |
NC_000009.10:g.129616284T>G | NCBI36 |
NG_009551.1:g.45585A>C , LRG_589:g.45585A>C | |
NG_023245.1:g.16310T>G |
HGVS | Amino-acid Change |
---|---|
ENST00000467826.5:n.710-24T>G | |
XM_005251864.2:c.1484-24T>G | XP_005251921.1:n.1484-24T>G |
XM_005251864.4:c.1484-24T>G | XP_005251921.1:n.1484-24T>G |
XM_017014565.2:c.1334-24T>G | XP_016870054.1:n.1334-24T>G |
XR_242582.2:n.1381-24T>G | |
XR_242582.4:n.1379-24T>G |