HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149569685A= , CM000664.2:g.149569685A= | GRCh38 |
NC_000002.11:g.150426199A= , CM000664.1:g.150426199A= | GRCh37 |
NC_000002.10:g.150134445A= | NCBI36 |
NG_009189.1:g.23132T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.*289T= MANE Select | ENSP00000301920.5:n.*289T= | |
ENST00000303319.9:c.*289T= | ENSP00000301920.5:n.*289T= | |
ENST00000422782.2:c.*289T= | ENSP00000408331.2:n.*289T= | |
ENST00000428879.5:c.*289T= | ENSP00000389060.1:n.*289T= | |
NM_015702.2:c.*289T= | NP_056517.1:n.*289T= | |
NM_015702.3:c.*289T= MANE Select | NP_056517.1:n.*289T= |