HGVS | Genome Assembly |
---|---|
NC_000017.11:g.40867168T>C , CM000679.2:g.40867168T>C | GRCh38 |
NC_000017.10:g.39023420T>C , CM000679.1:g.39023420T>C | GRCh37 |
NC_000017.9:g.36276946T>C | NCBI36 |
NG_008077.1:g.5043A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251643.5:c.19A>G MANE Select | ENSP00000251643.4:p.Thr7Ala | |
ENST00000647902.1:c.19A>G | ENSP00000497770.1:p.Thr7Ala | |
ENST00000251643.4:c.19A>G | ENSP00000251643.4:p.Thr7Ala | |
NM_000223.3:c.19A>G | NP_000214.1:p.Thr7Ala | |
XR_934754.1:n.1500+16308T>C | ||
XR_934754.2:n.2008+16308T>C | ||
NM_000223.4:c.19A>G MANE Select | NP_000214.1:p.Thr7Ala |