HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94775505C= , CM000672.2:g.94775505C= | GRCh38 |
NC_000010.10:g.96535262C= , CM000672.1:g.96535262C= | GRCh37 |
NC_000010.9:g.96525252C= | NCBI36 |
NG_008384.2:g.17800C= | |
NG_008384.3:g.17825C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.447C= MANE Select | ENSP00000360372.3:p.Ala149= | |
ENST00000645461.1:n.1500C= | ||
ENST00000371321.7:c.447C= | ENSP00000360372.3:p.Ala149= | |
ENST00000464755.1:c.1210C= | ENSP00000483243.1:n.1210C= | |
ENST00000480405.2:c.447C= | ENSP00000483847.1:p.Ala149= | |
NM_000769.2:c.447C= | NP_000760.1:p.Ala149= | |
NM_000769.4:c.447C= MANE Select | NP_000760.1:p.Ala149= |