Linked Data
ClinVar Variation Id:
258002
dbSNP Id:
rs775698729
ExAC:
5:13692251 A / C
gnomAD v2:
5-13692251-A-C
gnomAD v4:
5-13692142-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13692142A>C , CM000667.2:g.13692142A>C | GRCh38 |
| NC_000005.9:g.13692251A>C , CM000667.1:g.13692251A>C | GRCh37 |
| NC_000005.8:g.13745251A>C | NCBI36 |
| NG_013081.1:g.257339T>G | |
| NG_013081.2:g.257339T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000683611.1:n.1057-7T>G | ||
| ENST00000265104.5:c.13724-7T>G MANE Select | ENSP00000265104.4:n.13724-7T>G | |
| ENST00000681290.1:c.13679-7T>G | ENSP00000505288.1:n.13679-7T>G | |
| ENST00000265104.4:c.13724-7T>G | ENSP00000265104.4:n.13724-7T>G | |
| NM_001369.2:c.13724-7T>G | NP_001360.1:n.13724-7T>G | |
| XM_005248262.2:c.13679-7T>G | XP_005248319.1:n.13679-7T>G | |
| XM_005248262.3:c.13832-7T>G | XP_005248319.2:n.13832-7T>G | |
| XM_017009177.1:c.13412-7T>G | XP_016864666.1:n.13412-7T>G | |
| XM_017009178.1:c.12737-7T>G | XP_016864667.1:n.12737-7T>G | |
| XM_017009179.2:c.12737-7T>G | XP_016864668.1:n.12737-7T>G | |
| XM_017009185.1:c.8921-7T>G | XP_016864674.1:n.8921-7T>G | |
| XM_017009186.1:c.8474-7T>G | XP_016864675.1:n.8474-7T>G | |
| XM_017009188.1:c.7811-7T>G | XP_016864677.1:n.7811-7T>G | |
| XM_024454388.1:c.12737-7T>G | XP_024310156.1:n.12737-7T>G | |
| XM_024454389.1:c.12326-7T>G | XP_024310157.1:n.12326-7T>G | |
| NM_001369.3:c.13724-7T>G MANE Select | NP_001360.1:n.13724-7T>G |