HGVS | Genome Assembly |
---|---|
NC_000010.11:g.27404136T>G , CM000672.2:g.27404136T>G | GRCh38 |
NC_000010.10:g.27693065T>G , CM000672.1:g.27693065T>G | GRCh37 |
NC_000010.9:g.27733071T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000642324.1:c.1212-779A>C | ENSP00000495205.1:n.1212-779A>C | |
ENST00000438700.7:c.1212-779A>C | ENSP00000417658.2:n.1212-779A>C | |
ENST00000622555.1:c.1212-779A>C | ENSP00000479436.1:n.1212-779A>C | |
NM_001034842.3:c.1212-779A>C | NP_001030014.2:n.1212-779A>C | |
XM_005252449.2:c.1090-779A>C | XP_005252506.1:n.1090-779A>C | |
NM_001034842.4:c.1212-779A>C | NP_001030014.2:n.1212-779A>C | |
NM_001034842.5:c.1212-779A>C | NP_001030014.2:n.1212-779A>C | |
NM_001395743.1:c.1212-779A>C | NP_001382672.1:n.1212-779A>C |