Linked Data
gnomAD v4:
6-36676511-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.36676511C>T , CM000668.2:g.36676511C>T | GRCh38 |
| NC_000006.11:g.36644288C>T , CM000668.1:g.36644288C>T | GRCh37 |
| NC_000006.10:g.36752266C>T | NCBI36 |
| NG_009364.1:g.2830C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000448526.6:c.-51C>T | ENSP00000409259.3:n.-51C>T | |
| ENST00000615513.4:c.-19C>T | ENSP00000482768.1:n.-19C>T | |
| NM_001220777.1:c.-19C>T | NP_001207706.1:n.-19C>T | |
| NM_078467.2:c.-51C>T | NP_510867.1:n.-51C>T | |
| NM_001220777.2:c.-19C>T | NP_001207706.1:n.-19C>T | |
| NM_001291549.3:c.-201C>T | NP_001278478.1:n.-201C>T | |
| NM_001374509.1:c.-109C>T | NP_001361438.1:n.-109C>T | |
| NM_001374510.1:c.-26C>T | NP_001361439.1:n.-26C>T | |
| NM_078467.3:c.-51C>T | NP_510867.1:n.-51C>T |