HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102948020T>C , CM000673.2:g.102948020T>C | GRCh38 |
NC_000011.9:g.102818749T>C , CM000673.1:g.102818749T>C | GRCh37 |
NC_000011.8:g.102323959T>C | NCBI36 |
NG_021404.1:g.12715A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260302.8:c.1082A>G MANE Select | ENSP00000260302.3:p.Asp361Gly | |
ENST00000260302.7:c.1082A>G | ENSP00000260302.3:p.Asp361Gly | |
ENST00000340273.4:c.1082A>G | ENSP00000339672.4:p.Asp361Gly | |
ENST00000615555.4:c.1082A>G | ENSP00000482883.1:p.Asp361Gly | |
NM_002427.3:c.1082A>G | NP_002418.1:p.Asp361Gly | |
NM_002427.4:c.1082A>G MANE Select | NP_002418.1:p.Asp361Gly |