HGVS | Genome Assembly |
---|---|
NC_000005.10:g.151822550A>G , CM000667.2:g.151822550A>G | GRCh38 |
NC_000005.9:g.151202111A>G , CM000667.1:g.151202111A>G | GRCh37 |
NC_000005.8:g.151182304A>G | NCBI36 |
NG_011764.1:g.107287T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274576.9:c.*123T>C MANE Select | ENSP00000274576.5:n.*123T>C | |
ENST00000274576.8:c.*123T>C | ENSP00000274576.4:n.*123T>C | |
NM_000171.3:c.*123T>C | NP_000162.2:n.*123T>C | |
NM_001146040.1:c.*123T>C | NP_001139512.1:n.*123T>C | |
NM_001292000.1:c.*123T>C | NP_001278929.1:n.*123T>C | |
NM_000171.4:c.*123T>C MANE Select | NP_000162.2:n.*123T>C | |
NM_001146040.2:c.*123T>C | NP_001139512.1:n.*123T>C | |
NM_001292000.2:c.*123T>C | NP_001278929.1:n.*123T>C |