HGVS | Genome Assembly |
---|---|
NC_000009.12:g.86085247T>G , CM000671.2:g.86085247T>G | GRCh38 |
NC_000009.11:g.88700162T>G , CM000671.1:g.88700162T>G | GRCh37 |
NC_000009.10:g.87889982T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000388711.7:c.-21-5906A>C | ENSP00000373363.3:n.-21-5906A>C | |
ENST00000388712.7:c.-21-5906A>C MANE Select | ENSP00000373364.3:n.-21-5906A>C | |
ENST00000466178.1:c.-141-208A>C | ENSP00000418155.1:n.-141-208A>C | |
ENST00000472919.1:n.150-5906A>C | ||
NM_016548.3:c.-21-5906A>C | NP_057632.2:n.-21-5906A>C | |
NM_177937.2:c.-21-5906A>C | NP_808800.1:n.-21-5906A>C | |
NM_016548.4:c.-21-5906A>C MANE Select | NP_057632.2:n.-21-5906A>C | |
NM_177937.3:c.-21-5906A>C | NP_808800.1:n.-21-5906A>C |