HGVS | Genome Assembly |
---|---|
NC_000023.11:g.106036490T>G , CM000685.2:g.106036490T>G | GRCh38 |
NC_000023.10:g.105280481T>G , CM000685.1:g.105280481T>G | GRCh37 |
NC_000023.9:g.105167137T>G | NCBI36 |
NG_021252.1:g.7238A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000372563.2:c.569A>C MANE Select | ENSP00000361644.1:p.Gln190Pro | |
ENST00000327674.8:c.569A>C | ENSP00000329374.4:p.Gln190Pro | |
ENST00000372563.1:c.569A>C | ENSP00000361644.1:p.Gln190Pro | |
NM_000354.5:c.569A>C | NP_000345.2:p.Gln190Pro | |
XM_005262180.3:c.569A>C | XP_005262237.1:p.Gln190Pro | |
XM_006724683.1:c.569A>C | XP_006724746.1:p.Gln190Pro | |
XM_005262180.4:c.569A>C | XP_005262237.1:p.Gln190Pro | |
XM_006724683.2:c.569A>C | XP_006724746.1:p.Gln190Pro | |
NM_000354.6:c.569A>C MANE Select | NP_000345.2:p.Gln190Pro |