Linked Data
dbSNP Id:
rs1169811800
gnomAD v2:
17-70120035-C-T
gnomAD v3:
17-72123894-C-T
gnomAD v4:
17-72123894-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.72123894C>T , CM000679.2:g.72123894C>T | GRCh38 |
| NC_000017.10:g.70120035C>T , CM000679.1:g.70120035C>T | GRCh37 |
| NC_000017.9:g.67631630C>T | NCBI36 |
| NG_012490.1:g.7875C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245479.3:c.1037C>T MANE Select | ENSP00000245479.2:p.Pro346Leu | |
| ENST00000245479.2:c.1037C>T | ENSP00000245479.2:p.Pro346Leu | |
| NM_000346.3:c.1037C>T | NP_000337.1:p.Pro346Leu | |
| NM_000346.4:c.1037C>T MANE Select | NP_000337.1:p.Pro346Leu |