HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135132T>C , CM000664.2:g.26135132T>C | GRCh38 |
NC_000002.11:g.26358001T>C , CM000664.1:g.26358001T>C | GRCh37 |
NC_000002.10:g.26211505T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*111T>C MANE Select | ENSP00000264710.4:n.*111T>C | |
ENST00000264710.4:c.*111T>C | ENSP00000264710.4:n.*111T>C | |
ENST00000495146.5:n.1077T>C | ||
NM_016131.4:c.*111T>C | NP_057215.3:n.*111T>C | |
XM_024452565.1:c.*111T>C | XP_024308333.1:n.*111T>C | |
NM_016131.5:c.*111T>C MANE Select | NP_057215.3:n.*111T>C |