Linked Data
ClinVar Variation Id:
497563
dbSNP Id:
rs371225165
ExAC:
4:52890291 G / A
gnomAD v2:
4-52890291-G-A
gnomAD v3:
4-52024125-G-A
gnomAD v4:
4-52024125-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52024125G>A , CM000666.2:g.52024125G>A | GRCh38 |
| NC_000004.11:g.52890291G>A , CM000666.1:g.52890291G>A | GRCh37 |
| NC_000004.10:g.52585048G>A | NCBI36 |
| NG_008891.1:g.19195C>T , LRG_204:g.19195C>T | |
| NG_053164.1:g.1187C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.789C>T MANE Select | ENSP00000370839.6:p.Val263= | |
| ENST00000381431.9:c.789C>T | ENSP00000370839.5:p.Val263= | |
| NM_000232.4:c.789C>T , LRG_204t1:c.789C>T | NP_000223.1:p.Val263= | |
| XM_006714049.2:c.492C>T | XP_006714112.1:p.Val164= | |
| XM_011534403.1:c.579C>T | XP_011532705.1:p.Val193= | |
| XM_011534404.1:c.492C>T | XP_011532706.1:p.Val164= | |
| NM_000232.5:c.789C>T MANE Select | NP_000223.1:p.Val263= |