HGVS | Genome Assembly |
---|---|
NC_000017.11:g.61590745G>C , CM000679.2:g.61590745G>C | GRCh38 |
NC_000017.10:g.59668106G>C , CM000679.1:g.59668106G>C | GRCh37 |
NC_000017.9:g.57022888G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000521764.3:c.436C>G MANE Select | ENSP00000427802.1:p.Gln146Glu | |
ENST00000521764.2:c.436C>G | ENSP00000427802.1:p.Gln146Glu | |
NM_199290.3:c.436C>G | NP_954984.1:p.Gln146Glu | |
NM_199290.4:c.436C>G MANE Select | NP_954984.1:p.Gln146Glu |