HGVS | Genome Assembly |
---|---|
NC_000009.12:g.841871T>G , CM000671.2:g.841871T>G | GRCh38 |
NC_000009.11:g.841871T>G , CM000671.1:g.841871T>G | GRCh37 |
NC_000009.10:g.831871T>G | NCBI36 |
NG_009221.1:g.5182T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382276.8:c.33T>G MANE Select | ENSP00000371711.3:p.Ser11= | |
ENST00000382276.7:c.33T>G | ENSP00000371711.3:p.Ser11= | |
ENST00000564322.1:n.182T>G | ||
NM_021951.2:c.33T>G | NP_068770.2:p.Ser11= | |
XM_006716732.1:c.33T>G | XP_006716795.1:p.Ser11= | |
XM_017014375.1:c.33T>G | XP_016869864.1:p.Ser11= | |
NM_021951.3:c.33T>G MANE Select | NP_068770.2:p.Ser11= |