HGVS | Genome Assembly |
---|---|
NC_000006.12:g.29388554A>G , CM000668.2:g.29388554A>G | GRCh38 |
NC_000006.11:g.29356331A>G , CM000668.1:g.29356331A>G | GRCh37 |
NC_000006.10:g.29464310A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377154.1:c.-82-32277T>C | ENSP00000366359.1:n.-82-32277T>C | |
XM_011514929.1:c.-82-32277T>C | XP_011513231.1:n.-82-32277T>C | |
XM_011514930.1:c.-82-32277T>C | XP_011513232.1:n.-82-32277T>C | |
XM_011514931.1:c.-83+17464T>C | XP_011513233.1:n.-83+17464T>C | |
XM_011514932.1:c.-82-32277T>C | XP_011513234.1:n.-82-32277T>C | |
XM_011514930.2:c.-82-32277T>C | XP_011513232.1:n.-82-32277T>C | |
XM_024446562.1:c.-82-32277T>C | XP_024302330.1:n.-82-32277T>C |