Linked Data
gnomAD v4:
7-151187281-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.151187281C>A , CM000669.2:g.151187281C>A | GRCh38 |
| NC_000007.13:g.150884368C>A , CM000669.1:g.150884368C>A | GRCh37 |
| NC_000007.12:g.150515301C>A | NCBI36 |
| NG_017016.1:g.5552G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000275838.5:c.-151G>T | ENSP00000275838.1:n.-151G>T | |
| ENST00000377867.7:c.271+171G>T | ENSP00000367098.3:n.271+171G>T | |
| ENST00000415615.1:c.*94G>T | ENSP00000410871.1:n.*94G>T | |
| NM_001142459.1:c.-151G>T | NP_001135931.2:n.-151G>T | |
| NM_001142460.1:c.-151G>T | NP_001135932.2:n.-151G>T | |
| NM_080871.3:c.271+171G>T | NP_543147.2:n.271+171G>T | |
| NM_080871.4:c.271+171G>T | NP_543147.2:n.271+171G>T |