HGVS | Genome Assembly |
---|---|
NC_000009.12:g.27490969A>G , CM000671.2:g.27490969A>G | GRCh38 |
NC_000009.11:g.27490967A>G , CM000671.1:g.27490967A>G | GRCh37 |
NC_000009.10:g.27480967A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262244.6:c.-198-35221T>C MANE Select | ENSP00000262244.5:n.-198-35221T>C | |
ENST00000262244.5:c.-198-35221T>C | ENSP00000262244.5:n.-198-35221T>C | |
NM_024761.4:c.-198-35221T>C | NP_079037.3:n.-198-35221T>C | |
NM_024761.5:c.-198-35221T>C MANE Select | NP_079037.3:n.-198-35221T>C |