HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29328636T>C , CM000664.2:g.29328636T>C | GRCh38 |
NC_000002.11:g.29551502T>C , CM000664.1:g.29551502T>C | GRCh37 |
NC_000002.10:g.29405006T>C | NCBI36 |
NG_009445.1:g.597931A>G , LRG_488:g.597931A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389048.8:c.1283-155A>G MANE Select | ENSP00000373700.3:n.1283-155A>G | |
ENST00000389048.7:c.1283-155A>G | ENSP00000373700.3:n.1283-155A>G | |
ENST00000618119.4:c.152-155A>G | ENSP00000482733.1:n.152-155A>G | |
NM_004304.4:c.1283-155A>G | NP_004295.2:n.1283-155A>G | |
XR_939920.1:n.817+127T>C | ||
XR_939921.1:n.680+6108T>C | ||
XR_001738688.2:n.2213-155A>G | ||
XR_939920.2:n.707+127T>C | ||
XR_939921.2:n.576+6108T>C | ||
NM_004304.5:c.1283-155A>G MANE Select | NP_004295.2:n.1283-155A>G |