HGVS | Genome Assembly |
---|---|
NC_000003.12:g.133691793T>C , CM000665.2:g.133691793T>C | GRCh38 |
NC_000003.11:g.133410637T>C , CM000665.1:g.133410637T>C | GRCh37 |
NC_000003.10:g.134893327T>C | NCBI36 |
NG_013080.2:g.34796T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000460564.5:n.209+3429T>C (INHCAP) | ||
ENST00000475455.1:n.244T>C (INHCAP) | ||
ENST00000490470.5:n.209+3429T>C (INHCAP) | ||
ENST00000497521.5:n.208+3429T>C (INHCAP) | ||
XM_011513100.1:c.-1289+3429T>C (TF) | XP_011511402.1:n.-1289+3429T>C | |
NM_001354703.1:c.-940+3429T>C (TF) | NP_001341632.1:n.-940+3429T>C | |
NM_001354703.2:c.-940+3429T>C (TF) | NP_001341632.2:n.-940+3429T>C |