HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67753991T>G , CM000666.2:g.67753991T>G | GRCh38 |
NC_000004.11:g.68619709T>G , CM000666.1:g.68619709T>G | GRCh37 |
NC_000004.10:g.68302304T>G | NCBI36 |
NG_009293.1:g.7096A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.345A>C MANE Select | ENSP00000226413.5:p.Lys115Asn | |
ENST00000226413.4:c.345A>C | ENSP00000226413.4:p.Lys115Asn | |
ENST00000420975.2:c.345A>C | ENSP00000397561.2:p.Lys115Asn | |
NM_000406.2:c.345A>C | NP_000397.1:p.Lys115Asn | |
NM_001012763.1:c.345A>C | NP_001012781.1:p.Lys115Asn | |
NM_000406.3:c.345A>C MANE Select | NP_000397.1:p.Lys115Asn | |
NM_001012763.2:c.345A>C | NP_001012781.1:p.Lys115Asn |