Linked Data
ClinVar Variation Id:
329431
dbSNP Id:
rs782082118
ExAC:
19:42492463 G / A
gnomAD v2:
19-42492463-G-A
gnomAD v3:
19-41988311-G-A
gnomAD v4:
19-41988311-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41988311G>A , CM000681.2:g.41988311G>A | GRCh38 |
| NC_000019.9:g.42492463G>A , CM000681.1:g.42492463G>A | GRCh37 |
| NC_000019.8:g.47184303G>A | NCBI36 |
| NG_008015.1:g.10920C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545399.6:c.192+7C>T | ENSP00000444688.1:n.192+7C>T | |
| ENST00000644613.1:c.153+7C>T | ENSP00000494711.1:n.153+7C>T | |
| ENST00000648268.1:c.153+7C>T MANE Select | ENSP00000498113.1:n.153+7C>T | |
| ENST00000302102.9:c.153+7C>T | ENSP00000302397.5:n.153+7C>T | |
| ENST00000441343.5:c.153+7C>T | ENSP00000411503.1:n.153+7C>T | |
| ENST00000465007.1:n.149C>T | ||
| ENST00000468774.3:n.462+7C>T | ||
| ENST00000473086.3:c.63+7C>T | ENSP00000469129.2:n.63+7C>T | |
| ENST00000543770.5:c.186+7C>T | ENSP00000437577.1:n.186+7C>T | |
| ENST00000545399.5:c.192+7C>T | ENSP00000444688.1:n.192+7C>T | |
| ENST00000602133.5:c.63+7C>T | ENSP00000471581.1:n.63+7C>T | |
| NM_001256213.1:c.186+7C>T | NP_001243142.1:n.186+7C>T | |
| NM_001256214.1:c.192+7C>T | NP_001243143.1:n.192+7C>T | |
| NM_152296.4:c.153+7C>T | NP_689509.1:n.153+7C>T | |
| XM_011526991.1:c.63+7C>T | XP_011525293.1:n.63+7C>T | |
| NM_152296.5:c.153+7C>T MANE Select | NP_689509.1:n.153+7C>T | |
| NM_001256214.2:c.192+7C>T | NP_001243143.1:n.192+7C>T | |
| NM_001256213.2:c.186+7C>T | NP_001243142.1:n.186+7C>T |