HGVS | Genome Assembly |
---|---|
NC_000002.12:g.206122197A= , CM000664.2:g.206122197A= | GRCh38 |
NC_000002.11:g.206986921A= , CM000664.1:g.206986921A= | GRCh37 |
NC_000002.10:g.206695166A= | NCBI36 |
NG_009248.1:g.42267T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233190.11:c.*1988T= MANE Select | ENSP00000233190.5:n.*1988T= | |
ENST00000233190.10:c.*1988T= | ENSP00000233190.5:n.*1988T= | |
NM_001199981.2:c.*1988T= | NP_001186910.1:n.*1988T= | |
NM_001199982.2:c.*1988T= | NP_001186911.1:n.*1988T= | |
NM_001199983.2:c.*1988T= | NP_001186912.1:n.*1988T= | |
NM_005006.7:c.*1988T= MANE Select | NP_004997.4:n.*1988T= | |
NM_001199984.2:c.*1988T= | NP_001186913.1:n.*1988T= |