HGVS | Genome Assembly |
---|---|
NC_000004.12:g.69858065A>G , CM000666.2:g.69858065A>G | GRCh38 |
NC_000004.11:g.70723783A>G , CM000666.1:g.70723783A>G | GRCh37 |
NC_000004.10:g.70758372A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226444.4:c.-9-412T>C MANE Select | ENSP00000226444.3:n.-9-412T>C | |
ENST00000226444.3:c.-9-412T>C | ENSP00000226444.3:n.-9-412T>C | |
ENST00000504002.1:n.98-412T>C | ||
NM_005420.2:c.-9-412T>C | NP_005411.1:n.-9-412T>C | |
XM_011532209.1:c.-9-412T>C | XP_011530511.1:n.-9-412T>C | |
XM_011532210.1:c.-9-412T>C | XP_011530512.1:n.-9-412T>C | |
XM_011532210.2:c.-9-412T>C | XP_011530512.1:n.-9-412T>C | |
NM_005420.3:c.-9-412T>C MANE Select | NP_005411.1:n.-9-412T>C |