HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229432185G>C , CM000663.2:g.229432185G>C | GRCh38 |
NC_000001.10:g.229567932G>C , CM000663.1:g.229567932G>C | GRCh37 |
NC_000001.9:g.227634555G>C | NCBI36 |
NG_006672.1:g.6912C>G , LRG_429:g.6912C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000366683.4:c.617C>G | ENSP00000355644.4:p.Ala206Gly | |
ENST00000684723.1:c.482C>G | ENSP00000508084.1:p.Ala161Gly | |
ENST00000366683.3:c.479+222C>G | ENSP00000355644.3:n.479+222C>G | |
ENST00000366684.7:c.617C>G MANE Select | ENSP00000355645.3:p.Ala206Gly | |
NM_001100.3:c.617C>G , LRG_429t1:c.617C>G | NP_001091.1:p.Ala206Gly | |
NM_001100.4:c.617C>G MANE Select | NP_001091.1:p.Ala206Gly |