HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6167513T>G , CM000668.2:g.6167513T>G | GRCh38 |
NC_000006.11:g.6167746T>G , CM000668.1:g.6167746T>G | GRCh37 |
NC_000006.10:g.6112745T>G | NCBI36 |
NG_008107.1:g.158179A>C , LRG_549:g.158179A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264870.8:c.1853A>C MANE Select | ENSP00000264870.3:p.Asp618Ala | |
ENST00000264870.7:c.1853A>C | ENSP00000264870.3:p.Asp618Ala | |
NM_000129.3:c.1853A>C , LRG_549t1:c.1853A>C | NP_000120.2:p.Asp618Ala | |
XM_006715010.2:c.1853A>C | XP_006715073.1:p.Asp618Ala | |
XM_011514342.1:c.2015A>C | XP_011512644.1:p.Asp672Ala | |
NM_000129.4:c.1853A>C MANE Select | NP_000120.2:p.Asp618Ala |