HGVS | Genome Assembly |
---|---|
NC_000009.12:g.127854364C>G , CM000671.2:g.127854364C>G | GRCh38 |
NC_000009.11:g.130616643C>G , CM000671.1:g.130616643C>G | GRCh37 |
NC_000009.10:g.129656464C>G | NCBI36 |
NG_009551.1:g.5405G>C , LRG_589:g.5405G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373203.9:c.-9G>C MANE Select | ENSP00000362299.4:n.-9G>C | |
ENST00000344849.4:c.-9G>C | ENSP00000341917.3:n.-9G>C | |
ENST00000373203.8:c.-9G>C | ENSP00000362299.4:n.-9G>C | |
NM_000118.3:c.-9G>C , LRG_589t1:c.-9G>C | NP_000109.1:n.-9G>C | |
NM_001114753.2:c.-9G>C , LRG_589t2:c.-9G>C | NP_001108225.1:n.-9G>C | |
NM_001114753.3:c.-9G>C MANE Select | NP_001108225.1:n.-9G>C |