HGVS | Genome Assembly |
---|---|
NC_000002.12:g.85545855A>G , CM000664.2:g.85545855A>G | GRCh38 |
NC_000002.11:g.85772978A>G , CM000664.1:g.85772978A>G | GRCh37 |
NC_000002.10:g.85626489A>G | NCBI36 |
NG_011811.2:g.20680T>C | |
NG_029183.1:g.11878A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000233838.9:c.*4079T>C MANE Select | ENSP00000233838.3:n.*4079T>C | |
ENST00000233838.8:c.*4079T>C | ENSP00000233838.3:n.*4079T>C | |
NM_000821.5:c.*4079T>C | NP_000812.2:n.*4079T>C | |
NM_000821.6:c.*4079T>C | NP_000812.2:n.*4079T>C | |
NM_001142269.2:c.*4079T>C | NP_001135741.1:n.*4079T>C | |
NM_001142269.3:c.*4079T>C | NP_001135741.1:n.*4079T>C | |
NM_000821.7:c.*4079T>C MANE Select | NP_000812.2:n.*4079T>C | |
NM_001142269.4:c.*4079T>C | NP_001135741.1:n.*4079T>C |