HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8587813T>C , CM000685.2:g.8587813T>C | GRCh38 |
NC_000023.10:g.8555854T>C , CM000685.1:g.8555854T>C | GRCh37 |
NC_000023.9:g.8515854T>C | NCBI36 |
NG_007088.1:g.149374A>G | |
NG_007088.2:g.149374A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262648.8:c.707A>G MANE Select | ENSP00000262648.3:p.His236Arg | |
ENST00000262648.7:c.707A>G | ENSP00000262648.3:p.His236Arg | |
ENST00000619786.1:c.704A>G | ENSP00000478734.1:p.His235Arg | |
NM_000216.2:c.707A>G | NP_000207.2:p.His236Arg | |
XM_005274501.3:c.707A>G | XP_005274558.1:p.His236Arg | |
NM_000216.3:c.707A>G | NP_000207.2:p.His236Arg | |
XM_005274501.4:c.707A>G | XP_005274558.1:p.His236Arg | |
NM_000216.4:c.707A>G MANE Select | NP_000207.2:p.His236Arg |