HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135031386T>G , CM000667.2:g.135031386T>G | GRCh38 |
NC_000005.9:g.134367076T>G , CM000667.1:g.134367076T>G | GRCh37 |
NC_000005.8:g.134394975T>G | NCBI36 |
NG_012114.1:g.7889A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.292A>C MANE Select | ENSP00000265340.6:p.Ser98Arg | |
ENST00000265340.11:c.292A>C | ENSP00000265340.6:p.Ser98Arg | |
ENST00000502676.1:c.292A>C | ENSP00000423624.1:p.Ser98Arg | |
ENST00000503586.1:c.414A>C | ||
ENST00000504936.1:n.625A>C | ||
ENST00000506438.5:c.292A>C | ENSP00000427542.1:p.Ser98Arg | |
ENST00000507253.5:c.292A>C | ENSP00000422908.1:p.Ser98Arg | |
NM_002653.4:c.292A>C | NP_002644.4:p.Ser98Arg | |
NM_002653.5:c.292A>C MANE Select | NP_002644.4:p.Ser98Arg |