Linked Data
ClinVar Variation Id:
498849
dbSNP Id:
rs749798782
ExAC:
6:42936636 A / G
gnomAD v2:
6-42936636-A-G
gnomAD v3:
6-42968898-A-G
gnomAD v4:
6-42968898-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42968898A>G , CM000668.2:g.42968898A>G | GRCh38 |
| NC_000006.11:g.42936636A>G , CM000668.1:g.42936636A>G | GRCh37 |
| NC_000006.10:g.43044614A>G | NCBI36 |
| NG_008370.1:g.15346T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304611.13:c.1455T>C MANE Select | ENSP00000303511.8:p.Ser485= | |
| ENST00000244546.4:c.1455T>C | ENSP00000244546.4:p.Ser485= | |
| ENST00000304611.12:c.1455T>C | ENSP00000303511.8:p.Ser485= | |
| NM_000287.3:c.1455T>C | NP_000278.3:p.Ser485= | |
| NM_001316313.1:c.1191T>C | NP_001303242.1:p.Ser397= | |
| NR_133009.1:n.1548T>C | ||
| XM_011514661.1:c.1371T>C | XP_011512963.1:p.Ser457= | |
| XR_926246.1:n.1461-400T>C | ||
| XM_011514661.2:c.1371T>C | XP_011512963.1:p.Ser457= | |
| XR_001743466.2:n.2442-400T>C | ||
| NM_000287.4:c.1455T>C MANE Select | NP_000278.3:p.Ser485= | |
| NM_001316313.2:c.1191T>C | NP_001303242.1:p.Ser397= | |
| NR_133009.2:n.1486T>C |