HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52029727A= , CM000666.2:g.52029727A= | GRCh38 |
NC_000004.11:g.52895893A= , CM000666.1:g.52895893A= | GRCh37 |
NC_000004.10:g.52590650A= | NCBI36 |
NG_008891.1:g.13593T= , LRG_204:g.13593T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.380T= MANE Select | ENSP00000370839.6:p.Val127= | |
ENST00000381431.9:c.380T= | ENSP00000370839.5:p.Val127= | |
ENST00000506357.5:c.463T= | ||
ENST00000514133.1:c.457T= | ENSP00000425818.1:n.457T= | |
NM_000232.4:c.380T= , LRG_204t1:c.380T= | NP_000223.1:p.Val127= | |
XM_006714049.2:c.83T= | XP_006714112.1:p.Val28= | |
XM_011534403.1:c.170T= | XP_011532705.1:p.Val57= | |
XM_011534404.1:c.83T= | XP_011532706.1:p.Val28= | |
NM_000232.5:c.380T= MANE Select | NP_000223.1:p.Val127= |