HGVS | Genome Assembly |
---|---|
NC_000004.12:g.69858444C>A , CM000666.2:g.69858444C>A | GRCh38 |
NC_000004.11:g.70724162C>A , CM000666.1:g.70724162C>A | GRCh37 |
NC_000004.10:g.70758751C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226444.4:c.-9-791G>T MANE Select | ENSP00000226444.3:n.-9-791G>T | |
ENST00000226444.3:c.-9-791G>T | ENSP00000226444.3:n.-9-791G>T | |
ENST00000504002.1:n.98-791G>T | ||
NM_005420.2:c.-9-791G>T | NP_005411.1:n.-9-791G>T | |
XM_011532209.1:c.-9-791G>T | XP_011530511.1:n.-9-791G>T | |
XM_011532210.1:c.-9-791G>T | XP_011530512.1:n.-9-791G>T | |
XM_011532210.2:c.-9-791G>T | XP_011530512.1:n.-9-791G>T | |
NM_005420.3:c.-9-791G>T MANE Select | NP_005411.1:n.-9-791G>T |