HGVS | Genome Assembly |
---|---|
NC_000005.10:g.93585291G>C , CM000667.2:g.93585291G>C | GRCh38 |
NC_000005.9:g.92920997G>C , CM000667.1:g.92920997G>C | GRCh37 |
NC_000005.8:g.92946753G>C | NCBI36 |
NG_034119.1:g.6955G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000615873.2:c.193G>C | ENSP00000481517.1:p.Gly65Arg | |
ENST00000327111.8:c.268G>C MANE Select | ENSP00000325819.3:p.Gly90Arg | |
ENST00000647447.1:c.115G>C | ENSP00000495740.1:p.Gly39Arg | |
ENST00000327111.7:c.268G>C | ENSP00000325819.3:p.Gly90Arg | |
ENST00000615873.1:c.193G>C | ENSP00000481517.1:p.Gly65Arg | |
NM_005654.5:c.268G>C | NP_005645.1:p.Gly90Arg | |
NM_005654.6:c.268G>C MANE Select | NP_005645.1:p.Gly90Arg |