HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31859708A>G , CM000668.2:g.31859708A>G | GRCh38 |
NC_000006.11:g.31827485A>G , CM000668.1:g.31827485A>G | GRCh37 |
NC_000006.10:g.31935464A>G | NCBI36 |
NG_008201.1:g.8225T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375631.5:c.*11T>C MANE Select | ENSP00000364782.4:n.*11T>C | |
ENST00000677054.1:n.2598T>C | ||
ENST00000677512.1:n.1536T>C | ||
ENST00000678869.1:n.1847T>C | ||
ENST00000375631.4:c.*11T>C | ENSP00000364782.4:n.*11T>C | |
ENST00000480384.1:n.1558T>C | ||
ENST00000491768.5:c.*369T>C | ENSP00000433127.1:n.*369T>C | |
ENST00000495807.1:n.2567T>C | ||
NM_000434.3:c.*11T>C | NP_000425.1:n.*11T>C | |
NM_000434.4:c.*11T>C MANE Select | NP_000425.1:n.*11T>C |