HGVS | Genome Assembly |
---|---|
NC_000016.10:g.23417100A>C , CM000678.2:g.23417100A>C | GRCh38 |
NC_000016.9:g.23428421A>C , CM000678.1:g.23428421A>C | GRCh37 |
NC_000016.8:g.23335922A>C | NCBI36 |
NG_021287.1:g.41092T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307149.10:c.1159T>G MANE Select | ENSP00000305442.5:p.Cys387Gly | |
ENST00000307149.9:c.1159T>G | ENSP00000305442.5:p.Cys387Gly | |
ENST00000567821.1:n.194T>G | ||
NM_153603.3:c.1159T>G | NP_705831.1:p.Cys387Gly | |
XR_429680.1:n.1375T>G | ||
XM_017023870.1:c.964T>G | XP_016879359.1:p.Cys322Gly | |
XR_002957852.1:n.1380T>G | ||
XR_429680.2:n.1380T>G | ||
NM_153603.4:c.1159T>G MANE Select | NP_705831.1:p.Cys387Gly |