Linked Data
gnomAD v4:
1-152305036-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152305036C>A , CM000663.2:g.152305036C>A | GRCh38 |
| NC_000001.10:g.152277512C>A , CM000663.1:g.152277512C>A | GRCh37 |
| NC_000001.9:g.150544136C>A | NCBI36 |
| NG_016190.1:g.25168G>T , LRG_1028:g.25168G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.9850G>T MANE Select | ENSP00000357789.1:p.Gly3284Cys | |
| ENST00000368799.1:c.9850G>T | ENSP00000357789.1:p.Gly3284Cys | |
| NM_002016.1:c.9850G>T , LRG_1028t1:c.9850G>T | NP_002007.1:p.Gly3284Cys | |
| XM_011509329.1:c.9108+742G>T | XP_011507631.1:n.9108+742G>T | |
| NM_002016.2:c.9850G>T MANE Select | NP_002007.1:p.Gly3284Cys |