HGVS | Genome Assembly |
---|---|
NC_000007.14:g.151187287T>A , CM000669.2:g.151187287T>A | GRCh38 |
NC_000007.13:g.150884374T>A , CM000669.1:g.150884374T>A | GRCh37 |
NC_000007.12:g.150515307T>A | NCBI36 |
NG_017016.1:g.5546A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000275838.5:c.-157A>T | ENSP00000275838.1:n.-157A>T | |
ENST00000377867.7:c.271+165A>T | ENSP00000367098.3:n.271+165A>T | |
ENST00000415615.1:c.*88A>T | ENSP00000410871.1:n.*88A>T | |
NM_001142459.1:c.-157A>T | NP_001135931.2:n.-157A>T | |
NM_001142460.1:c.-157A>T | NP_001135932.2:n.-157A>T | |
NM_080871.3:c.271+165A>T | NP_543147.2:n.271+165A>T | |
NM_080871.4:c.271+165A>T | NP_543147.2:n.271+165A>T |