HGVS | Genome Assembly |
---|---|
NC_000004.12:g.69858429A>T , CM000666.2:g.69858429A>T | GRCh38 |
NC_000004.11:g.70724147A>T , CM000666.1:g.70724147A>T | GRCh37 |
NC_000004.10:g.70758736A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226444.4:c.-9-776T>A MANE Select | ENSP00000226444.3:n.-9-776T>A | |
ENST00000226444.3:c.-9-776T>A | ENSP00000226444.3:n.-9-776T>A | |
ENST00000504002.1:n.98-776T>A | ||
NM_005420.2:c.-9-776T>A | NP_005411.1:n.-9-776T>A | |
XM_011532209.1:c.-9-776T>A | XP_011530511.1:n.-9-776T>A | |
XM_011532210.1:c.-9-776T>A | XP_011530512.1:n.-9-776T>A | |
XM_011532210.2:c.-9-776T>A | XP_011530512.1:n.-9-776T>A | |
NM_005420.3:c.-9-776T>A MANE Select | NP_005411.1:n.-9-776T>A |