HGVS | Genome Assembly |
---|---|
NC_000023.11:g.121048316A>C , CM000685.2:g.121048316A>C | GRCh38 |
NC_000023.10:g.120182170A>C , CM000685.1:g.120182170A>C | GRCh37 |
NC_000023.9:g.120009851A>C | NCBI36 |
NG_016456.1:g.5709A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000328078.3:c.632A>C MANE Select | ENSP00000327589.1:p.Lys211Thr | |
ENST00000328078.2:c.632A>C | ENSP00000327589.1:p.Lys211Thr | |
NM_012084.3:c.632A>C | NP_036216.2:p.Lys211Thr | |
NM_012084.4:c.632A>C MANE Select | NP_036216.2:p.Lys211Thr |