Linked Data
gnomAD v4:
3-147413660-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.147413660C>T , CM000665.2:g.147413660C>T | GRCh38 |
| NC_000003.11:g.147131447C>T , CM000665.1:g.147131447C>T | GRCh37 |
| NC_000003.10:g.148614137C>T | NCBI36 |
| NG_015886.1:g.9267C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282928.5:c.*109C>T MANE Select | ENSP00000282928.4:n.*109C>T | |
| ENST00000282928.4:c.*109C>T | ENSP00000282928.4:n.*109C>T | |
| ENST00000472523.1:n.521+19718C>T | ||
| ENST00000488404.5:c.519C>T | ||
| NM_003412.3:c.*109C>T | NP_003403.2:n.*109C>T | |
| NM_003412.4:c.*109C>T MANE Select | NP_003403.2:n.*109C>T |