Linked Data
dbSNP Id:
rs761889405
ExAC:
18:7015784 C / T
gnomAD v2:
18-7015784-C-T
gnomAD v4:
18-7015785-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.7015785C>T , CM000680.2:g.7015785C>T | GRCh38 |
| NC_000018.9:g.7015784C>T , CM000680.1:g.7015784C>T | GRCh37 |
| NC_000018.8:g.7005784C>T | NCBI36 |
| NG_034251.1:g.107030G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389658.4:c.3063G>A MANE Select | ENSP00000374309.3:p.Gln1021= | |
| ENST00000389658.3:c.3063G>A | ENSP00000374309.3:p.Gln1021= | |
| ENST00000579014.5:n.4078G>A | ||
| NM_005559.3:c.3063G>A | NP_005550.2:p.Gln1021= | |
| XM_011525655.1:c.3063G>A | XP_011523957.1:p.Gln1021= | |
| XM_011525656.1:c.1491G>A | XP_011523958.1:p.Gln497= | |
| XM_011525657.1:c.3063G>A | XP_011523959.1:p.Gln1021= | |
| XM_011525655.2:c.3063G>A | XP_011523957.1:p.Gln1021= | |
| XM_011525656.2:c.1491G>A | XP_011523958.1:p.Gln497= | |
| NM_005559.4:c.3063G>A MANE Select | NP_005550.2:p.Gln1021= |