Linked Data
dbSNP Id:
rs1043620924
gnomAD v2:
6-149608890-C-T
gnomAD v3:
6-149287754-C-T
gnomAD v4:
6-149287754-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.149287754C>T , CM000668.2:g.149287754C>T | GRCh38 |
| NC_000006.11:g.149608890C>T , CM000668.1:g.149608890C>T | GRCh37 |
| NC_000006.10:g.149650583C>T | NCBI36 |
| NG_021386.2:g.74831C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000606202.1:c.-121+68978C>T | ENSP00000476139.1:n.-121+68978C>T | |
| NM_001292035.2:c.6+68978C>T | NP_001278964.1:n.6+68978C>T | |
| NM_001292035.3:c.6+68978C>T | NP_001278964.1:n.6+68978C>T |