HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69350225A>G , CM000674.2:g.69350225A>G | GRCh38 |
NC_000012.11:g.69744005A>G , CM000674.1:g.69744005A>G | GRCh37 |
NC_000012.10:g.68030272A>G | NCBI36 |
NG_008195.1:g.6872A>G , LRG_768:g.6872A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.254A>G MANE Select | ENSP00000261267.2:p.Asp85Gly | |
ENST00000261267.6:c.254A>G | ENSP00000261267.2:p.Asp85Gly | |
ENST00000548839.1:c.254A>G | ENSP00000449969.1:p.Asp85Gly | |
ENST00000549690.1:c.254A>G | ENSP00000449898.1:p.Asp85Gly | |
NM_000239.2:c.254A>G , LRG_768t1:c.254A>G | NP_000230.1:p.Asp85Gly | |
NM_000239.3:c.254A>G MANE Select | NP_000230.1:p.Asp85Gly |