HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60648694T>C , CM000676.2:g.60648694T>C | GRCh38 |
NC_000014.8:g.61115412T>C , CM000676.1:g.61115412T>C | GRCh37 |
NC_000014.7:g.60185165T>C | NCBI36 |
NG_008231.1:g.5744A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645694.3:c.496A>G (SIX1) MANE Select | ENSP00000494686.1:p.Thr166Ala | |
ENST00000247182.6:c.496A>G (SIX1) | ENSP00000247182.5:p.Thr166Ala | |
ENST00000553535.2:n.249-2117A>G (SIX1) | ||
ENST00000554986.2:c.42-2117A>G (SIX1) | ENSP00000452700.2:n.42-2117A>G | |
ENST00000555955.3:n.1198-2117A>G (SIX1) | ||
NM_005982.3:c.496A>G (SIX1) | NP_005973.1:p.Thr166Ala | |
XM_017021602.2:c.496A>G (SIX1) | XP_016877091.1:p.Thr166Ala | |
NM_005982.4:c.496A>G (SIX1) MANE Select | NP_005973.1:p.Thr166Ala | |
NR_162089.1:n.47T>C (MIR9718) |