HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154860442C>G , CM000685.2:g.154860442C>G | GRCh38 |
NC_000023.10:g.154088717C>G , CM000685.1:g.154088717C>G | GRCh37 |
NC_000023.9:g.153741911C>G | NCBI36 |
NG_011403.1:g.167282G>C | |
NG_011403.2:g.167282G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.6890G>C MANE Select | ENSP00000353393.4:p.Gly2297Ala | |
ENST00000644698.1:c.623G>C | ENSP00000495706.1:p.Gly208Ala | |
ENST00000330287.10:c.485G>C | ENSP00000327895.6:p.Gly162Ala | |
ENST00000360256.8:c.6890G>C | ENSP00000353393.4:p.Gly2297Ala | |
NM_000132.3:c.6890G>C | NP_000123.1:p.Gly2297Ala | |
NM_019863.2:c.485G>C | NP_063916.1:p.Gly162Ala | |
XM_011531126.1:c.6785G>C | XP_011529428.1:p.Gly2262Ala | |
NM_000132.4:c.6890G>C MANE Select | NP_000123.1:p.Gly2297Ala | |
NM_019863.3:c.485G>C | NP_063916.1:p.Gly162Ala |