HGVS | Genome Assembly |
---|---|
NC_000004.12:g.69858232T>C , CM000666.2:g.69858232T>C | GRCh38 |
NC_000004.11:g.70723950T>C , CM000666.1:g.70723950T>C | GRCh37 |
NC_000004.10:g.70758539T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226444.4:c.-9-579A>G MANE Select | ENSP00000226444.3:n.-9-579A>G | |
ENST00000226444.3:c.-9-579A>G | ENSP00000226444.3:n.-9-579A>G | |
ENST00000504002.1:n.98-579A>G | ||
NM_005420.2:c.-9-579A>G | NP_005411.1:n.-9-579A>G | |
XM_011532209.1:c.-9-579A>G | XP_011530511.1:n.-9-579A>G | |
XM_011532210.1:c.-9-579A>G | XP_011530512.1:n.-9-579A>G | |
XM_011532210.2:c.-9-579A>G | XP_011530512.1:n.-9-579A>G | |
NM_005420.3:c.-9-579A>G MANE Select | NP_005411.1:n.-9-579A>G |