HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67753837T>C , CM000666.2:g.67753837T>C | GRCh38 |
NC_000004.11:g.68619555T>C , CM000666.1:g.68619555T>C | GRCh37 |
NC_000004.10:g.68302150T>C | NCBI36 |
NG_009293.1:g.7250A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000226413.5:c.499A>G MANE Select | ENSP00000226413.5:p.Ser167Gly | |
ENST00000226413.4:c.499A>G | ENSP00000226413.4:p.Ser167Gly | |
ENST00000420975.2:c.499A>G | ENSP00000397561.2:p.Ser167Gly | |
NM_000406.2:c.499A>G | NP_000397.1:p.Ser167Gly | |
NM_001012763.1:c.499A>G | NP_001012781.1:p.Ser167Gly | |
NM_000406.3:c.499A>G MANE Select | NP_000397.1:p.Ser167Gly | |
NM_001012763.2:c.499A>G | NP_001012781.1:p.Ser167Gly |