HGVS | Genome Assembly |
---|---|
NC_000002.12:g.85546512T>C , CM000664.2:g.85546512T>C | GRCh38 |
NC_000002.11:g.85773635T>C , CM000664.1:g.85773635T>C | GRCh37 |
NC_000002.10:g.85627146T>C | NCBI36 |
NG_011811.2:g.20023A>G | |
NG_029183.1:g.12535T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000233838.9:c.*3422A>G MANE Select | ENSP00000233838.3:n.*3422A>G | |
ENST00000233838.8:c.*3422A>G | ENSP00000233838.3:n.*3422A>G | |
NM_000821.5:c.*3422A>G | NP_000812.2:n.*3422A>G | |
NM_000821.6:c.*3422A>G | NP_000812.2:n.*3422A>G | |
NM_001142269.2:c.*3422A>G | NP_001135741.1:n.*3422A>G | |
NM_001142269.3:c.*3422A>G | NP_001135741.1:n.*3422A>G | |
NM_000821.7:c.*3422A>G MANE Select | NP_000812.2:n.*3422A>G | |
NM_001142269.4:c.*3422A>G | NP_001135741.1:n.*3422A>G |