HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134835157T>A , CM000671.2:g.134835157T>A | GRCh38 |
NC_000009.11:g.137727003T>A , CM000671.1:g.137727003T>A | GRCh37 |
NC_000009.10:g.136866824T>A | NCBI36 |
NG_008030.1:g.198352T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371820.4:c.5323T>A | ENSP00000360885.4:p.Ser1775Thr | |
ENST00000371817.8:c.5323T>A MANE Select | ENSP00000360882.3:p.Ser1775Thr | |
ENST00000371817.7:c.5323T>A | ENSP00000360882.3:p.Ser1775Thr | |
ENST00000371820.3:c.581T>A | ||
ENST00000618395.4:c.5323T>A | ENSP00000481360.1:p.Ser1775Thr | |
NM_000093.4:c.5323T>A | NP_000084.3:p.Ser1775Thr | |
NM_001278074.1:c.5323T>A | NP_001265003.1:p.Ser1775Thr | |
NR_103451.2:n.71-14948A>T | ||
NM_000093.5:c.5323T>A MANE Select | NP_000084.3:p.Ser1775Thr |