Linked Data
dbSNP Id:
rs1343938352
gnomAD v2:
12-52845349-T-C
gnomAD v3:
12-52451565-T-C
gnomAD v4:
12-52451565-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52451565T>C , CM000674.2:g.52451565T>C | GRCh38 |
| NC_000012.11:g.52845349T>C , CM000674.1:g.52845349T>C | GRCh37 |
| NC_000012.10:g.51131616T>C | NCBI36 |
| NG_008299.1:g.5562A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252252.4:c.514A>G MANE Select | ENSP00000252252.3:p.Asn172Asp | |
| ENST00000252252.3:c.514A>G | ENSP00000252252.3:p.Asn172Asp | |
| NM_005555.3:c.514A>G | NP_005546.2:p.Asn172Asp | |
| NM_005555.4:c.514A>G MANE Select | NP_005546.2:p.Asn172Asp |