Linked Data
ClinVar Variation Id:
450082
ClinVar RCV Id:
RCV001696923
dbSNP Id:
rs1556464851
gnomAD v4:
X-37783493-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37783493G>A , CM000685.2:g.37783493G>A | GRCh38 |
| NC_000023.10:g.37642746G>A , CM000685.1:g.37642746G>A | GRCh37 |
| NC_000023.9:g.37527690G>A | NCBI36 |
| NG_009065.1:g.8477G>A , LRG_53:g.8477G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696170.1:c.145G>A | ENSP00000512461.1:p.Ala49Thr | |
| ENST00000696171.1:c.49G>A | ENSP00000512462.1:p.Ala17Thr | |
| ENST00000696172.1:c.145G>A | ENSP00000512463.1:p.Ala49Thr | |
| ENST00000696173.1:n.153G>A | ||
| ENST00000378588.5:c.145G>A MANE Select | ENSP00000367851.4:p.Ala49Thr | |
| ENST00000378588.4:c.145G>A | ENSP00000367851.4:p.Ala49Thr | |
| ENST00000465127.1:c.171+357493G>A | ENSP00000417050.1:n.171+357493G>A | |
| NM_000397.3:c.145G>A , LRG_53t1:c.145G>A | NP_000388.2:p.Ala49Thr | |
| XM_011543890.1:c.-286G>A | XP_011542192.1:n.-286G>A | |
| NM_000397.4:c.145G>A MANE Select | NP_000388.2:p.Ala49Thr |