HGVS | Genome Assembly |
---|---|
NC_000009.12:g.78304930G>T , CM000671.2:g.78304930G>T | GRCh38 |
NC_000009.11:g.80919846G>T , CM000671.1:g.80919846G>T | GRCh37 |
NC_000009.10:g.80109666G>T | NCBI36 |
NG_012165.1:g.12788G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376588.4:c.387G>T MANE Select | ENSP00000365773.3:p.Gly129= | |
ENST00000347159.6:c.387G>T | ENSP00000317606.2:p.Gly129= | |
ENST00000376588.3:c.387G>T | ENSP00000365773.3:p.Gly129= | |
NM_021154.4:c.387G>T | NP_066977.1:p.Gly129= | |
NM_058179.3:c.387G>T | NP_478059.1:p.Gly129= | |
NM_058179.4:c.387G>T MANE Select | NP_478059.1:p.Gly129= | |
NM_021154.5:c.387G>T | NP_066977.1:p.Gly129= |