HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233652T>G , CM000667.2:g.55233652T>G | GRCh38 |
NC_000005.9:g.54529480T>G , CM000667.1:g.54529480T>G | GRCh37 |
NC_000005.8:g.54565237T>G | NCBI36 |
NG_034201.1:g.5066A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.4:c.-129A>C | ENSP00000282572.4:n.-129A>C | |
NM_021147.4:c.-129A>C | NP_066970.3:n.-129A>C | |
NR_125346.1:n.66A>C | ||
NR_125347.1:n.66A>C |