HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189004015C>G , CM000664.2:g.189004015C>G | GRCh38 |
NC_000002.11:g.189868741C>G , CM000664.1:g.189868741C>G | GRCh37 |
NC_000002.10:g.189576986C>G | NCBI36 |
NG_007404.1:g.34643C>G , LRG_3:g.34643C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.2596C>G | ENSP00000415346.2:p.Pro866Ala | |
ENST00000304636.9:c.2695C>G MANE Select | ENSP00000304408.4:p.Pro899Ala | |
ENST00000304636.7:c.2695C>G | ENSP00000304408.3:p.Pro899Ala | |
ENST00000317840.9:c.2527+979C>G | ENSP00000315243.6:n.2527+979C>G | |
NM_000090.3:c.2695C>G , LRG_3t1:c.2695C>G | NP_000081.1:p.Pro899Ala | |
NM_000090.4:c.2695C>G MANE Select | NP_000081.2:p.Pro899Ala |