HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67754065T>C , CM000666.2:g.67754065T>C | GRCh38 |
NC_000004.11:g.68619783T>C , CM000666.1:g.68619783T>C | GRCh37 |
NC_000004.10:g.68302378T>C | NCBI36 |
NG_009293.1:g.7022A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.271A>G MANE Select | ENSP00000226413.5:p.Thr91Ala | |
ENST00000226413.4:c.271A>G | ENSP00000226413.4:p.Thr91Ala | |
ENST00000420975.2:c.271A>G | ENSP00000397561.2:p.Thr91Ala | |
NM_000406.2:c.271A>G | NP_000397.1:p.Thr91Ala | |
NM_001012763.1:c.271A>G | NP_001012781.1:p.Thr91Ala | |
NM_000406.3:c.271A>G MANE Select | NP_000397.1:p.Thr91Ala | |
NM_001012763.2:c.271A>G | NP_001012781.1:p.Thr91Ala |