HGVS | Genome Assembly |
---|---|
NC_000017.11:g.61590607T>C , CM000679.2:g.61590607T>C | GRCh38 |
NC_000017.10:g.59667968T>C , CM000679.1:g.59667968T>C | GRCh37 |
NC_000017.9:g.57022750T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000521764.3:c.574A>G MANE Select | ENSP00000427802.1:p.Arg192Gly | |
ENST00000521764.2:c.574A>G | ENSP00000427802.1:p.Arg192Gly | |
NM_199290.3:c.574A>G | NP_954984.1:p.Arg192Gly | |
NM_199290.4:c.574A>G MANE Select | NP_954984.1:p.Arg192Gly |