HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52027979C>G , CM000666.2:g.52027979C>G | GRCh38 |
NC_000004.11:g.52894145C>G , CM000666.1:g.52894145C>G | GRCh37 |
NC_000004.10:g.52588902C>G | NCBI36 |
NG_008891.1:g.15341G>C , LRG_204:g.15341G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000381431.10:c.742G>C MANE Select | ENSP00000370839.6:p.Glu248Gln | |
ENST00000381431.9:c.742G>C | ENSP00000370839.5:p.Glu248Gln | |
NM_000232.4:c.742G>C , LRG_204t1:c.742G>C | NP_000223.1:p.Glu248Gln | |
XM_006714049.2:c.445G>C | XP_006714112.1:p.Glu149Gln | |
XM_011534403.1:c.532G>C | XP_011532705.1:p.Glu178Gln | |
XM_011534404.1:c.445G>C | XP_011532706.1:p.Glu149Gln | |
NM_000232.5:c.742G>C MANE Select | NP_000223.1:p.Glu248Gln |