Linked Data
gnomAD v4:
2-240868657-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868657C>T , CM000664.2:g.240868657C>T | GRCh38 |
| NC_000002.11:g.241808074C>T , CM000664.1:g.241808074C>T | GRCh37 |
| NC_000002.10:g.241456747C>T | NCBI36 |
| NG_008005.1:g.4913C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.3:c.-209C>T | ENSP00000302620.3:n.-209C>T | |
| XR_924060.1:n.405+1576G>A |