HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7528943C= , CM000681.2:g.7528943C= | GRCh38 |
NC_000019.9:g.7593829C= , CM000681.1:g.7593829C= | GRCh37 |
NC_000019.8:g.7499829C= | NCBI36 |
NG_015806.1:g.11334C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.1107C= MANE Select | ENSP00000264079.5:p.Thr369= | |
ENST00000264079.10:c.1107C= | ENSP00000264079.5:p.Thr369= | |
ENST00000394321.9:n.1422C= | ||
ENST00000595860.5:n.290C= | ||
NM_020533.2:c.1107C= | NP_065394.1:p.Thr369= | |
NM_020533.3:c.1107C= MANE Select | NP_065394.1:p.Thr369= |