Linked Data
dbSNP Id:
rs782495015
ExAC:
X:154185223 A / C
gnomAD v2:
X-154185223-A-C
gnomAD v4:
X-154956948-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154956948A>C , CM000685.2:g.154956948A>C | GRCh38 |
| NC_000023.10:g.154185223A>C , CM000685.1:g.154185223A>C | GRCh37 |
| NC_000023.9:g.153838417A>C | NCBI36 |
| NG_011403.1:g.70776T>G | |
| NG_011403.2:g.70776T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.1752+9T>G MANE Select | ENSP00000353393.4:n.1752+9T>G | |
| ENST00000647125.1:c.*1628+9T>G | ENSP00000496062.1:n.*1628+9T>G | |
| ENST00000360256.8:c.1752+9T>G | ENSP00000353393.4:n.1752+9T>G | |
| NM_000132.3:c.1752+9T>G | NP_000123.1:n.1752+9T>G | |
| XM_011531126.1:c.1647+9T>G | XP_011529428.1:n.1647+9T>G | |
| NM_000132.4:c.1752+9T>G MANE Select | NP_000123.1:n.1752+9T>G |