HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63957435A>G , CM000679.2:g.63957435A>G | GRCh38 |
NC_000017.10:g.62034795A>G , CM000679.1:g.62034795A>G | GRCh37 |
NC_000017.9:g.59388527A>G | NCBI36 |
NG_011699.1:g.20484T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000435607.3:c.2103T>C MANE Select | ENSP00000396320.1:p.Gly701= | |
ENST00000578147.5:c.2103T>C | ENSP00000463963.1:p.Gly701= | |
NM_000334.4:c.2103T>C MANE Select | NP_000325.4:p.Gly701= | |
XM_005257566.3:c.2103T>C | XP_005257623.1:p.Gly701= |