Linked Data
dbSNP Id:
rs566674173
ExAC:
2:21246410 A / T
gnomAD v2:
2-21246410-A-T
gnomAD v3:
2-21023538-A-T
gnomAD v4:
2-21023538-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21023538A>T , CM000664.2:g.21023538A>T | GRCh38 |
| NC_000002.11:g.21246410A>T , CM000664.1:g.21246410A>T | GRCh37 |
| NC_000002.10:g.21099915A>T | NCBI36 |
| NG_011793.1:g.25536T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673739.2:c.*1897T>A | ENSP00000501110.2:n.*1897T>A | |
| ENST00000673882.2:c.*1897T>A | ENSP00000501253.2:n.*1897T>A | |
| ENST00000673739.1:c.2305T>A | ENSP00000501110.1:n.2305T>A | |
| ENST00000673882.1:c.2305T>A | ENSP00000501253.1:n.2305T>A | |
| ENST00000233242.5:c.2591T>A MANE Select | ENSP00000233242.1:p.Leu864Gln | |
| ENST00000616098.4:c.2591T>A | ENSP00000477990.1:p.Leu864Gln | |
| NM_000384.2:c.2591T>A | NP_000375.2:p.Leu864Gln | |
| XM_011532809.1:c.2591T>A | XP_011531111.1:p.Leu864Gln | |
| NM_000384.3:c.2591T>A MANE Select | NP_000375.3:p.Leu864Gln |