HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713913A>G , CM000663.2:g.114713913A>G | GRCh38 |
NC_000001.10:g.115256534A>G , CM000663.1:g.115256534A>G | GRCh37 |
NC_000001.9:g.115058057A>G | NCBI36 |
NG_007572.1:g.7982T>C , LRG_92:g.7982T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.177T>C MANE Select | ENSP00000358548.4:p.Ala59= | |
ENST00000369535.4:c.177T>C | ENSP00000358548.4:p.Ala59= | |
NM_002524.4:c.177T>C | NP_002515.1:p.Ala59= | |
NM_002524.5:c.177T>C MANE Select | NP_002515.1:p.Ala59= |