HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134731537G= , CM000671.2:g.134731537G= | GRCh38 |
NC_000009.11:g.137623383G= , CM000671.1:g.137623383G= | GRCh37 |
NC_000009.10:g.136763204G= | NCBI36 |
NG_008030.1:g.94732G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371820.4:c.1206G= | ENSP00000360885.4:p.Gly402= | |
ENST00000371817.8:c.1206G= MANE Select | ENSP00000360882.3:p.Gly402= | |
ENST00000371817.7:c.1206G= | ENSP00000360882.3:p.Gly402= | |
ENST00000618395.4:c.1206G= | ENSP00000481360.1:p.Gly402= | |
NM_000093.4:c.1206G= | NP_000084.3:p.Gly402= | |
NM_001278074.1:c.1206G= | NP_001265003.1:p.Gly402= | |
XR_929712.1:n.1608G= | ||
XR_929713.1:n.1608G= | ||
XM_017014266.2:c.1206G= | XP_016869755.1:p.Gly402= | |
XR_001746183.1:n.1604G= | ||
NM_000093.5:c.1206G= MANE Select | NP_000084.3:p.Gly402= |