Linked Data
ClinVar Variation Id:
644453
ClinVar RCV Id:
RCV000798371
dbSNP Id:
rs1377720264
gnomAD v2:
3-49160295-C-G
gnomAD v4:
3-49122862-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49122862C>G , CM000665.2:g.49122862C>G | GRCh38 |
| NC_000003.11:g.49160295C>G , CM000665.1:g.49160295C>G | GRCh37 |
| NC_000003.10:g.49135299C>G | NCBI36 |
| NG_008094.1:g.15305G>C | |
| NG_054716.1:g.3077G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305544.9:c.4415G>C MANE Select | ENSP00000307156.4:p.Ser1472Thr | |
| ENST00000305544.8:c.4415G>C | ENSP00000307156.4:p.Ser1472Thr | |
| ENST00000418109.5:c.4415G>C | ENSP00000388325.1:p.Ser1472Thr | |
| ENST00000469665.1:n.724G>C | ||
| NM_002292.3:c.4415G>C | NP_002283.3:p.Ser1472Thr | |
| XM_005265127.3:c.4415G>C | XP_005265184.1:p.Ser1472Thr | |
| XM_005265127.4:c.4415G>C | XP_005265184.1:p.Ser1472Thr | |
| NM_002292.4:c.4415G>C MANE Select | NP_002283.3:p.Ser1472Thr |