Linked Data
gnomAD v4:
2-240868629-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868629T>C , CM000664.2:g.240868629T>C | GRCh38 |
| NC_000002.11:g.241808046T>C , CM000664.1:g.241808046T>C | GRCh37 |
| NC_000002.10:g.241456719T>C | NCBI36 |
| NG_008005.1:g.4885T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.3:c.-237T>C | ENSP00000302620.3:n.-237T>C | |
| XR_924060.1:n.405+1604A>G |