HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81314963G= , CM000678.2:g.81314963G= | GRCh38 |
NC_000016.9:g.81348568G= , CM000678.1:g.81348568G= | GRCh37 |
NC_000016.8:g.79906069G= | NCBI36 |
NG_009007.1:g.4998G= , LRG_242:g.4998G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.-151G= | ENSP00000498114.1:n.-151G= | |
ENST00000648994.2:c.-151G= MANE Select | ENSP00000497351.1:n.-151G= | |
ENST00000568107.2:c.-151G= | ENSP00000476795.1:n.-151G= | |
XM_017023734.1:c.-675G= | XP_016879223.1:n.-675G= | |
NM_001377486.1:c.-675G= | NP_001364415.1:n.-675G= | |
NM_022041.4:c.-151G= MANE Select | NP_071324.1:n.-151G= |