HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218893304T>G , CM000664.2:g.218893304T>G | GRCh38 |
NC_000002.11:g.219758026T>G , CM000664.1:g.219758026T>G | GRCh37 |
NC_000002.10:g.219466270T>G | NCBI36 |
NG_012179.1:g.17772T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258411.8:c.*33T>G MANE Select | ENSP00000258411.3:n.*33T>G | |
ENST00000258411.7:c.*33T>G | ENSP00000258411.3:n.*33T>G | |
ENST00000489887.1:n.47+37T>G | ||
NM_025216.2:c.*33T>G | NP_079492.2:n.*33T>G | |
XM_011511928.1:c.*33T>G | XP_011510230.1:n.*33T>G | |
XM_011511929.1:c.*33T>G | XP_011510231.1:n.*33T>G | |
XM_011511930.1:c.*7T>G | XP_011510232.1:n.*7T>G | |
XM_011511929.2:c.*33T>G | XP_011510231.1:n.*33T>G | |
NM_025216.3:c.*33T>G MANE Select | NP_079492.2:n.*33T>G |