HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21174708T= , CM000674.2:g.21174708T= | GRCh38 |
NC_000012.11:g.21327642T= , CM000674.1:g.21327642T= | GRCh37 |
NC_000012.10:g.21218909T= | NCBI36 |
NG_011745.1:g.48515T= , LRG_1022:g.48515T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.358T= MANE Select | ENSP00000256958.2:p.Tyr120= | |
ENST00000256958.2:c.358T= | ENSP00000256958.2:p.Tyr120= | |
ENST00000543498.5:c.426-2068T= | ||
NM_006446.4:c.358T= , LRG_1022t1:c.358T= | NP_006437.3:p.Tyr120= | |
NM_006446.5:c.358T= MANE Select | NP_006437.3:p.Tyr120= |