HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114709572T>C , CM000663.2:g.114709572T>C | GRCh38 |
NC_000001.10:g.115252193T>C , CM000663.1:g.115252193T>C | GRCh37 |
NC_000001.9:g.115053716T>C | NCBI36 |
NG_007572.1:g.12323A>G , LRG_92:g.12323A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.447A>G MANE Select | ENSP00000358548.4:p.Arg149= | |
ENST00000369535.4:c.447A>G | ENSP00000358548.4:p.Arg149= | |
NM_002524.4:c.447A>G | NP_002515.1:p.Arg149= | |
NM_002524.5:c.447A>G MANE Select | NP_002515.1:p.Arg149= |