HGVS | Genome Assembly |
---|---|
NC_000006.12:g.34762518T>C , CM000668.2:g.34762518T>C | GRCh38 |
NC_000006.11:g.34730295T>C , CM000668.1:g.34730295T>C | GRCh37 |
NC_000006.10:g.34838273T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000244520.10:c.52-77T>C MANE Select | ENSP00000244520.5:n.52-77T>C | |
ENST00000244520.9:c.52-77T>C | ENSP00000244520.5:n.52-77T>C | |
ENST00000374017.3:c.115-77T>C | ENSP00000363129.3:n.115-77T>C | |
ENST00000374018.5:c.-72-77T>C | ENSP00000363130.1:n.-72-77T>C | |
ENST00000474635.1:n.44-77T>C | ||
NM_003093.2:c.52-77T>C | NP_003084.1:n.52-77T>C | |
NR_029472.1:n.459-77T>C | ||
NM_003093.3:c.52-77T>C MANE Select | NP_003084.1:n.52-77T>C | |
NR_029472.2:n.48-77T>C |