Linked Data
ClinVar Variation Id:
728827
ClinVar RCV Id:
RCV000903374
dbSNP Id:
rs565428084
ExAC:
7:42005488 G / C
gnomAD v2:
7-42005488-G-C
gnomAD v3:
7-41965890-G-C
gnomAD v4:
7-41965890-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41965890G>C , CM000669.2:g.41965890G>C | GRCh38 |
| NC_000007.13:g.42005488G>C , CM000669.1:g.42005488G>C | GRCh37 |
| NC_000007.12:g.41972013G>C | NCBI36 |
| NG_008434.1:g.276131C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395925.8:c.3183C>G MANE Select | ENSP00000379258.3:p.His1061Gln | |
| ENST00000677288.1:c.3009C>G | ENSP00000503986.1:p.His1003Gln | |
| ENST00000677605.1:c.3183C>G | ENSP00000503743.1:p.His1061Gln | |
| ENST00000678429.1:c.3183C>G | ENSP00000502957.1:p.His1061Gln | |
| ENST00000395925.7:c.3183C>G | ENSP00000379258.3:p.His1061Gln | |
| ENST00000479210.1:n.3160C>G | ||
| NM_000168.5:c.3183C>G | NP_000159.3:p.His1061Gln | |
| XM_005249703.1:c.3183C>G | XP_005249760.1:p.His1061Gln | |
| XM_005249704.2:c.3183C>G | XP_005249761.1:p.His1061Gln | |
| XM_011515272.1:c.3183C>G | XP_011513574.1:p.His1061Gln | |
| XM_011515273.1:c.3183C>G | XP_011513575.1:p.His1061Gln | |
| XM_011515274.1:c.3006C>G | XP_011513576.1:p.His1002Gln | |
| XM_011515274.2:c.3006C>G | XP_011513576.1:p.His1002Gln | |
| XM_017011997.1:c.3180C>G | XP_016867486.1:p.His1060Gln | |
| NM_000168.6:c.3183C>G MANE Select | NP_000159.3:p.His1061Gln |