HGVS | Genome Assembly |
---|---|
NC_000002.12:g.176118978C>G , CM000664.2:g.176118978C>G | GRCh38 |
NC_000002.11:g.176983706C>G , CM000664.1:g.176983706C>G | GRCh37 |
NC_000002.10:g.176691952C>G | NCBI36 |
NG_008133.2:g.12215C>G , LRG_246:g.12215C>G | |
NG_009225.1:g.1294C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000249501.5:c.770C>G MANE Select | ENSP00000249501.4:p.Thr257Ser | |
ENST00000249501.4:c.770C>G | ENSP00000249501.4:p.Thr257Ser | |
ENST00000490088.2:n.594C>G | ||
ENST00000549469.1:n.641C>G | ||
NM_002148.3:c.770C>G , LRG_246t1:c.770C>G | NP_002139.2:p.Thr257Ser | |
NM_002148.4:c.770C>G MANE Select | NP_002139.2:p.Thr257Ser |