HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96251308A>G , CM000664.2:g.96251308A>G | GRCh38 |
NC_000002.11:g.96917046A>G , CM000664.1:g.96917046A>G | GRCh37 |
NC_000002.10:g.96280773A>G | NCBI36 |
NG_027695.1:g.19706T>C , LRG_528:g.19706T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258439.8:c.*2500T>C MANE Select | ENSP00000258439.3:n.*2500T>C | |
ENST00000258439.7:c.*2500T>C | ENSP00000258439.2:n.*2500T>C | |
NM_001193304.2:c.*2500T>C | NP_001180233.1:n.*2500T>C | |
NM_017849.3:c.*2500T>C , LRG_528t1:c.*2500T>C | NP_060319.1:n.*2500T>C | |
XM_017004450.1:c.*1801T>C | XP_016859939.1:n.*1801T>C | |
XM_017004452.1:c.*2500T>C | XP_016859941.1:n.*2500T>C | |
NM_001193304.3:c.*2500T>C | NP_001180233.1:n.*2500T>C | |
NM_017849.4:c.*2500T>C MANE Select | NP_060319.1:n.*2500T>C |