HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1443771T>C , CM000667.2:g.1443771T>C | GRCh38 |
NC_000005.9:g.1443886T>C , CM000667.1:g.1443886T>C | GRCh37 |
NC_000005.8:g.1496886T>C | NCBI36 |
NG_015885.1:g.6658A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.-45-529A>G MANE Select | ENSP00000270349.9:n.-45-529A>G | |
ENST00000270349.11:c.-45-529A>G | ENSP00000270349.9:n.-45-529A>G | |
NM_001044.4:c.-45-529A>G | NP_001035.1:n.-45-529A>G | |
NM_001044.5:c.-45-529A>G MANE Select | NP_001035.1:n.-45-529A>G |