HGVS | Genome Assembly |
---|---|
NC_000005.10:g.178994954T>C , CM000667.2:g.178994954T>C | GRCh38 |
NC_000005.9:g.178421955T>C , CM000667.1:g.178421955T>C | GRCh37 |
NC_000005.8:g.178354561T>C | NCBI36 |
NG_008105.1:g.5170A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000517717.3:c.-10A>G MANE Select | ENSP00000430767.1:n.-10A>G | |
ENST00000650031.1:c.-10A>G | ENSP00000497110.1:n.-10A>G | |
ENST00000231188.9:c.-10A>G | ENSP00000231188.5:n.-10A>G | |
ENST00000517717.1:c.-10A>G | ENSP00000430767.1:n.-10A>G | |
NM_000843.3:c.-10A>G | NP_000834.2:n.-10A>G | |
NM_000843.4:c.-10A>G MANE Select | NP_000834.2:n.-10A>G |