HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29328790A>T , CM000664.2:g.29328790A>T | GRCh38 |
NC_000002.11:g.29551656A>T , CM000664.1:g.29551656A>T | GRCh37 |
NC_000002.10:g.29405160A>T | NCBI36 |
NG_009445.1:g.597777T>A , LRG_488:g.597777T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389048.8:c.1283-309T>A MANE Select | ENSP00000373700.3:n.1283-309T>A | |
ENST00000389048.7:c.1283-309T>A | ENSP00000373700.3:n.1283-309T>A | |
ENST00000618119.4:c.152-309T>A | ENSP00000482733.1:n.152-309T>A | |
NM_004304.4:c.1283-309T>A | NP_004295.2:n.1283-309T>A | |
XR_939920.1:n.818-135A>T | ||
XR_939921.1:n.680+6262A>T | ||
XR_001738688.2:n.2213-309T>A | ||
XR_939920.2:n.708-135A>T | ||
XR_939921.2:n.576+6262A>T | ||
NM_004304.5:c.1283-309T>A MANE Select | NP_004295.2:n.1283-309T>A |