Linked Data
ClinVar Variation Id:
286988
dbSNP Id:
rs79625212
ExAC:
7:42004111 C / T
gnomAD v2:
7-42004111-C-T
gnomAD v4:
7-41964513-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41964513C>T , CM000669.2:g.41964513C>T | GRCh38 |
| NC_000007.13:g.42004111C>T , CM000669.1:g.42004111C>T | GRCh37 |
| NC_000007.12:g.41970636C>T | NCBI36 |
| NG_008434.1:g.277508G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395925.8:c.4560G>A MANE Select | ENSP00000379258.3:p.Ser1520= | |
| ENST00000677288.1:c.4386G>A | ENSP00000503986.1:p.Ser1462= | |
| ENST00000677605.1:c.4560G>A | ENSP00000503743.1:p.Ser1520= | |
| ENST00000678429.1:c.4560G>A | ENSP00000502957.1:p.Ser1520= | |
| ENST00000395925.7:c.4560G>A | ENSP00000379258.3:p.Ser1520= | |
| ENST00000479210.1:n.4537G>A | ||
| NM_000168.5:c.4560G>A | NP_000159.3:p.Ser1520= | |
| XM_005249703.1:c.4560G>A | XP_005249760.1:p.Ser1520= | |
| XM_005249704.2:c.4560G>A | XP_005249761.1:p.Ser1520= | |
| XM_011515272.1:c.4560G>A | XP_011513574.1:p.Ser1520= | |
| XM_011515273.1:c.4560G>A | XP_011513575.1:p.Ser1520= | |
| XM_011515274.1:c.4383G>A | XP_011513576.1:p.Ser1461= | |
| XM_011515274.2:c.4383G>A | XP_011513576.1:p.Ser1461= | |
| XM_017011997.1:c.4557G>A | XP_016867486.1:p.Ser1519= | |
| NM_000168.6:c.4560G>A MANE Select | NP_000159.3:p.Ser1520= |