Linked Data
gnomAD v4:
7-151187298-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.151187298G>T , CM000669.2:g.151187298G>T | GRCh38 |
| NC_000007.13:g.150884385G>T , CM000669.1:g.150884385G>T | GRCh37 |
| NC_000007.12:g.150515318G>T | NCBI36 |
| NG_017016.1:g.5535C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000275838.5:c.-168C>A | ENSP00000275838.1:n.-168C>A | |
| ENST00000377867.7:c.271+154C>A | ENSP00000367098.3:n.271+154C>A | |
| ENST00000415615.1:c.*77C>A | ENSP00000410871.1:n.*77C>A | |
| NM_001142459.1:c.-168C>A | NP_001135931.2:n.-168C>A | |
| NM_001142460.1:c.-168C>A | NP_001135932.2:n.-168C>A | |
| NM_080871.3:c.271+154C>A | NP_543147.2:n.271+154C>A | |
| NM_080871.4:c.271+154C>A | NP_543147.2:n.271+154C>A |