HGVS | Genome Assembly |
---|---|
NC_000004.12:g.154751600G>T , CM000666.2:g.154751600G>T | GRCh38 |
NC_000004.11:g.155672752G>T , CM000666.1:g.155672752G>T | GRCh37 |
NC_000004.10:g.155892202G>T | NCBI36 |
NG_009110.1:g.12590G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000336356.4:c.*2464G>T MANE Select | ENSP00000337224.3:n.*2464G>T | |
ENST00000336356.3:c.*2464G>T | ENSP00000337224.3:n.*2464G>T | |
ENST00000510733.1:n.3484G>T | ||
NM_001301645.1:c.*2464G>T | NP_001288574.1:n.*2464G>T | |
NM_004744.4:c.*2464G>T | NP_004735.2:n.*2464G>T | |
NM_004744.5:c.*2464G>T MANE Select | NP_004735.2:n.*2464G>T | |
NM_001301645.2:c.*2464G>T | NP_001288574.1:n.*2464G>T |