Linked Data
dbSNP Id:
rs1029908562
gnomAD v3:
2-233250141-T-C
gnomAD v4:
2-233250141-T-C
MyVariant Identifiers:
chr2:g.233250141T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233250141T>C , CM000664.2:g.233250141T>C | GRCh38 |
| NC_000002.11:g.234158787T>C , CM000664.1:g.234158787T>C | GRCh37 |
| NC_000002.10:g.233823526T>C | NCBI36 |
| NG_023038.1:g.3571T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000431917.5:c.-137-5961T>C | ENSP00000397512.1:n.-137-5961T>C |