Linked Data
ClinVar Variation Id:
3073028
ClinVar RCV Id:
RCV004015042
dbSNP Id:
rs767786832
ExAC:
15:48779408 A / G
gnomAD v2:
15-48779408-A-G
gnomAD v4:
15-48487211-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48487211A>G , CM000677.2:g.48487211A>G | GRCh38 |
| NC_000015.9:g.48779408A>G , CM000677.1:g.48779408A>G | GRCh37 |
| NC_000015.8:g.46566700A>G | NCBI36 |
| NG_008805.2:g.163578T>C , LRG_778:g.163578T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.3464-11T>C | ENSP00000453958.2:n.3464-11T>C | |
| ENST00000674301.2:c.3464-11T>C | ENSP00000501333.2:n.3464-11T>C | |
| ENST00000684448.1:n.2138-11T>C | ||
| ENST00000316623.10:c.3464-11T>C MANE Select | ENSP00000325527.5:n.3464-11T>C | |
| ENST00000316623.9:c.3464-11T>C | ENSP00000325527.5:n.3464-11T>C | |
| ENST00000537463.6:c.637-12561T>C | ENSP00000440294.2:n.637-12561T>C | |
| NM_000138.4:c.3464-11T>C , LRG_778t1:c.3464-11T>C | NP_000129.3:n.3464-11T>C | |
| NM_000138.5:c.3464-11T>C MANE Select | NP_000129.3:n.3464-11T>C |