HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136673611G>C , CM000671.2:g.136673611G>C | GRCh38 |
NC_000009.11:g.139568063G>C , CM000671.1:g.139568063G>C | GRCh37 |
NC_000009.10:g.138687884G>C | NCBI36 |
NG_008090.1:g.18849C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.*141C>G MANE Select | ENSP00000360761.2:n.*141C>G | |
ENST00000371694.7:c.*141C>G | ENSP00000360759.3:n.*141C>G | |
ENST00000371696.6:c.*141C>G | ENSP00000360761.2:n.*141C>G | |
ENST00000538402.1:c.*141C>G | ENSP00000438919.1:n.*141C>G | |
NM_001012727.1:c.*141C>G | NP_001012745.1:n.*141C>G | |
NM_006412.3:c.*141C>G | NP_006403.2:n.*141C>G | |
NM_006412.4:c.*141C>G MANE Select | NP_006403.2:n.*141C>G | |
NM_001012727.2:c.*141C>G | NP_001012745.1:n.*141C>G |