HGVS | Genome Assembly |
---|---|
NC_000017.11:g.40867156A>C , CM000679.2:g.40867156A>C | GRCh38 |
NC_000017.10:g.39023408A>C , CM000679.1:g.39023408A>C | GRCh37 |
NC_000017.9:g.36276934A>C | NCBI36 |
NG_008077.1:g.5055T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251643.5:c.31T>G MANE Select | ENSP00000251643.4:p.Ser11Ala | |
ENST00000647902.1:c.31T>G | ENSP00000497770.1:p.Ser11Ala | |
ENST00000251643.4:c.31T>G | ENSP00000251643.4:p.Ser11Ala | |
NM_000223.3:c.31T>G | NP_000214.1:p.Ser11Ala | |
XR_934754.1:n.1500+16296A>C | ||
XR_934754.2:n.2008+16296A>C | ||
NM_000223.4:c.31T>G MANE Select | NP_000214.1:p.Ser11Ala |