HGVS | Genome Assembly |
---|---|
NC_000020.11:g.59030339G= , CM000682.2:g.59030339G= | GRCh38 |
NC_000020.10:g.57605394G= , CM000682.1:g.57605394G= | GRCh37 |
NC_000020.9:g.57038789G= | NCBI36 |
NG_031871.1:g.7029C= | |
NG_031871.2:g.7029C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000243997.8:c.123C= MANE Select | ENSP00000243997.3:p.Ser41= | |
ENST00000243997.7:c.123C= | ENSP00000243997.3:p.Ser41= | |
ENST00000395659.1:c.123C= | ENSP00000379019.1:p.Ser41= | |
ENST00000395663.1:c.123C= | ENSP00000379023.1:p.Ser41= | |
NM_006886.3:c.123C= | NP_008817.1:p.Ser41= | |
NR_037929.1:n.827C= | ||
NR_037930.1:n.568C= | ||
NM_006886.4:c.123C= MANE Select | NP_008817.1:p.Ser41= |