HGVS | Genome Assembly |
---|---|
NC_000010.11:g.99845667C>A , CM000672.2:g.99845667C>A | GRCh38 |
NC_000010.10:g.101605424C>A , CM000672.1:g.101605424C>A | GRCh37 |
NC_000010.9:g.101595414C>A | NCBI36 |
NG_011798.1:g.67962C>A | |
NG_011798.2:g.68070C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647814.1:c.4031C>A MANE Select | ENSP00000497274.1:p.Thr1344Lys | |
ENST00000649459.1:n.379C>A | ||
ENST00000370449.8:c.4031C>A | ENSP00000359478.4:p.Thr1344Lys | |
NM_000392.4:c.4031C>A | NP_000383.1:p.Thr1344Lys | |
XM_006717630.2:c.3335C>A | XP_006717693.1:p.Thr1112Lys | |
XR_945604.1:n.4177-16C>A | ||
XR_945605.1:n.4095C>A | ||
NM_000392.5:c.4031C>A MANE Select | NP_000383.2:p.Thr1344Lys | |
XM_006717630.3:c.3335C>A | XP_006717693.1:p.Thr1112Lys | |
XR_945604.3:n.4231-16C>A | ||
XR_945605.3:n.4147C>A |