HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149569748T>C , CM000664.2:g.149569748T>C | GRCh38 |
NC_000002.11:g.150426262T>C , CM000664.1:g.150426262T>C | GRCh37 |
NC_000002.10:g.150134508T>C | NCBI36 |
NG_009189.1:g.23069A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.*226A>G MANE Select | ENSP00000301920.5:n.*226A>G | |
ENST00000303319.9:c.*226A>G | ENSP00000301920.5:n.*226A>G | |
ENST00000422782.2:c.*226A>G | ENSP00000408331.2:n.*226A>G | |
ENST00000428879.5:c.*226A>G | ENSP00000389060.1:n.*226A>G | |
NM_015702.2:c.*226A>G | NP_056517.1:n.*226A>G | |
NM_015702.3:c.*226A>G MANE Select | NP_056517.1:n.*226A>G |