HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149569973G= , CM000664.2:g.149569973G= | GRCh38 |
NC_000002.11:g.150426487G= , CM000664.1:g.150426487G= | GRCh37 |
NC_000002.10:g.150134733G= | NCBI36 |
NG_009189.1:g.22844C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.*1C= MANE Select | ENSP00000301920.5:n.*1C= | |
ENST00000303319.9:c.*1C= | ENSP00000301920.5:n.*1C= | |
ENST00000422782.2:c.*1C= | ENSP00000408331.2:n.*1C= | |
ENST00000428879.5:c.*1C= | ENSP00000389060.1:n.*1C= | |
NM_015702.2:c.*1C= | NP_056517.1:n.*1C= | |
NM_015702.3:c.*1C= MANE Select | NP_056517.1:n.*1C= |