Linked Data
gnomAD v4:
2-240868698-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868698C>T , CM000664.2:g.240868698C>T | GRCh38 |
| NC_000002.11:g.241808115C>T , CM000664.1:g.241808115C>T | GRCh37 |
| NC_000002.10:g.241456788C>T | NCBI36 |
| NG_008005.1:g.4954C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.3:c.-168C>T | ENSP00000302620.3:n.-168C>T | |
| XR_924060.1:n.405+1535G>A |