HGVS | Genome Assembly |
---|---|
NC_000005.10:g.178994933G>C , CM000667.2:g.178994933G>C | GRCh38 |
NC_000005.9:g.178421934G>C , CM000667.1:g.178421934G>C | GRCh37 |
NC_000005.8:g.178354540G>C | NCBI36 |
NG_008105.1:g.5191C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000517717.3:c.12C>G MANE Select | ENSP00000430767.1:p.Pro4= | |
ENST00000650031.1:c.12C>G | ENSP00000497110.1:p.Pro4= | |
ENST00000231188.9:c.12C>G | ENSP00000231188.5:p.Pro4= | |
ENST00000517717.1:c.12C>G | ENSP00000430767.1:p.Pro4= | |
NM_000843.3:c.12C>G | NP_000834.2:p.Pro4= | |
NM_000843.4:c.12C>G MANE Select | NP_000834.2:p.Pro4= |