HGVS | Genome Assembly |
---|---|
NC_000002.12:g.85546757A>C , CM000664.2:g.85546757A>C | GRCh38 |
NC_000002.11:g.85773880A>C , CM000664.1:g.85773880A>C | GRCh37 |
NC_000002.10:g.85627391A>C | NCBI36 |
NG_011811.2:g.19778T>G | |
NG_029183.1:g.12780A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233838.9:c.*3177T>G MANE Select | ENSP00000233838.3:n.*3177T>G | |
ENST00000233838.8:c.*3177T>G | ENSP00000233838.3:n.*3177T>G | |
NM_000821.5:c.*3177T>G | NP_000812.2:n.*3177T>G | |
NM_000821.6:c.*3177T>G | NP_000812.2:n.*3177T>G | |
NM_001142269.2:c.*3177T>G | NP_001135741.1:n.*3177T>G | |
NM_001142269.3:c.*3177T>G | NP_001135741.1:n.*3177T>G | |
NM_000821.7:c.*3177T>G MANE Select | NP_000812.2:n.*3177T>G | |
NM_001142269.4:c.*3177T>G | NP_001135741.1:n.*3177T>G |