HGVS | Genome Assembly |
---|---|
NC_000012.12:g.92802646T>G , CM000674.2:g.92802646T>G | GRCh38 |
NC_000012.11:g.93196422T>G , CM000674.1:g.93196422T>G | GRCh37 |
NC_000012.10:g.91720553T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000322349.13:c.2428A>C MANE Select | ENSP00000317955.8:p.Lys810Gln | |
ENST00000322349.12:c.2428A>C | ENSP00000317955.8:p.Lys810Gln | |
XM_011538814.1:c.2554A>C | XP_011537116.1:p.Lys852Gln | |
XM_011538815.1:c.2290A>C | XP_011537117.1:p.Lys764Gln | |
XM_011538816.1:c.2554A>C | XP_011537118.1:p.Lys852Gln | |
XM_011538814.2:c.2554A>C | XP_011537116.1:p.Lys852Gln | |
XM_011538815.2:c.2290A>C | XP_011537117.1:p.Lys764Gln | |
XM_017020018.1:c.2446A>C | XP_016875507.1:p.Lys816Gln | |
NM_003566.4:c.2428A>C MANE Select | NP_003557.3:p.Lys810Gln |