HGVS | Genome Assembly |
---|---|
NC_000013.11:g.52397918G= , CM000675.2:g.52397918G= | GRCh38 |
NC_000013.10:g.52972053G= , CM000675.1:g.52972053G= | GRCh37 |
NC_000013.9:g.51870054G= | NCBI36 |
NG_047168.1:g.13577C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258613.5:c.335C= MANE Select | ENSP00000258613.4:p.Thr112= | |
ENST00000648254.1:c.335C= | ENSP00000497520.1:p.Thr112= | |
ENST00000258613.4:c.335C= | ENSP00000258613.4:p.Thr112= | |
ENST00000349258.8:c.335C= | ENSP00000340650.4:p.Thr112= | |
NM_018676.3:c.335C= | NP_061146.1:p.Thr112= | |
NM_199263.2:c.335C= | NP_954872.1:p.Thr112= | |
NM_018676.4:c.335C= MANE Select | NP_061146.1:p.Thr112= | |
NM_199263.3:c.335C= | NP_954872.1:p.Thr112= |