HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91055833G>C , CM000674.2:g.91055833G>C | GRCh38 |
NC_000012.11:g.91449610G>C , CM000674.1:g.91449610G>C | GRCh37 |
NC_000012.10:g.89973741G>C | NCBI36 |
NG_021223.1:g.7522C>G , LRG_538:g.7522C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266719.4:c.449C>G MANE Select | ENSP00000266719.3:p.Ala150Gly | |
ENST00000266719.3:c.449C>G | ENSP00000266719.3:p.Ala150Gly | |
NM_007035.3:c.449C>G , LRG_538t1:c.449C>G | NP_008966.1:p.Ala150Gly | |
XM_011537781.1:c.449C>G | XP_011536083.1:p.Ala150Gly | |
NM_007035.4:c.449C>G MANE Select | NP_008966.1:p.Ala150Gly |