HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43774188G= , CM000683.2:g.43774188G= | GRCh38 |
NC_000021.8:g.45194069G= , CM000683.1:g.45194069G= | GRCh37 |
NC_000021.7:g.44018497G= | NCBI36 |
NG_011545.1:g.7191C= , LRG_485:g.7191C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291568.7:c.*14C= MANE Select | ENSP00000291568.6:n.*14C= | |
ENST00000480147.3:n.2081C= | ||
ENST00000639959.1:c.178C= | ||
ENST00000640406.1:c.*386C= | ENSP00000492672.1:n.*386C= | |
ENST00000675996.1:n.736C= | ||
ENST00000291568.5:c.*14C= | ENSP00000291568.5:n.*14C= | |
NM_000100.3:c.*14C= , LRG_485t1:c.*14C= | NP_000091.1:n.*14C= | |
NM_000100.4:c.*14C= MANE Select | NP_000091.1:n.*14C= |