HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240868891C>T , CM000664.2:g.240868891C>T | GRCh38 |
NC_000002.11:g.241808308C>T , CM000664.1:g.241808308C>T | GRCh37 |
NC_000002.10:g.241456981C>T | NCBI36 |
NG_008005.1:g.5147C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.26C>T MANE Select | ENSP00000302620.3:p.Thr9Ile | |
ENST00000307503.3:c.26C>T | ENSP00000302620.3:p.Thr9Ile | |
ENST00000472436.1:n.46C>T | ||
NM_000030.2:c.26C>T | NP_000021.1:p.Thr9Ile | |
XR_924060.1:n.405+1342G>A | ||
NM_000030.3:c.26C>T MANE Select | NP_000021.1:p.Thr9Ile |