HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52029738A>T , CM000666.2:g.52029738A>T | GRCh38 |
NC_000004.11:g.52895904A>T , CM000666.1:g.52895904A>T | GRCh37 |
NC_000004.10:g.52590661A>T | NCBI36 |
NG_008891.1:g.13582T>A , LRG_204:g.13582T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.369T>A MANE Select | ENSP00000370839.6:p.Tyr123Ter | |
ENST00000381431.9:c.369T>A | ENSP00000370839.5:p.Tyr123Ter | |
ENST00000506357.5:c.452T>A | ||
ENST00000514133.1:c.446T>A | ENSP00000425818.1:n.446T>A | |
NM_000232.4:c.369T>A , LRG_204t1:c.369T>A | NP_000223.1:p.Tyr123Ter | |
XM_006714049.2:c.72T>A | XP_006714112.1:p.Tyr24Ter | |
XM_011534403.1:c.159T>A | XP_011532705.1:p.Tyr53Ter | |
XM_011534404.1:c.72T>A | XP_011532706.1:p.Tyr24Ter | |
NM_000232.5:c.369T>A MANE Select | NP_000223.1:p.Tyr123Ter |