Linked Data
ClinVar Variation Id:
287905
dbSNP Id:
rs748602445
ExAC:
4:52895019 G / A
gnomAD v2:
4-52895019-G-A
gnomAD v3:
4-52028853-G-A
gnomAD v4:
4-52028853-G-A
COSMIC:
COSM284942
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028853G>A , CM000666.2:g.52028853G>A | GRCh38 |
| NC_000004.11:g.52895019G>A , CM000666.1:g.52895019G>A | GRCh37 |
| NC_000004.10:g.52589776G>A | NCBI36 |
| NG_008891.1:g.14467C>T , LRG_204:g.14467C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.498C>T MANE Select | ENSP00000370839.6:p.Ile166= | |
| ENST00000381431.9:c.498C>T | ENSP00000370839.5:p.Ile166= | |
| ENST00000506357.5:c.581C>T | ||
| ENST00000514133.1:c.575C>T | ENSP00000425818.1:n.575C>T | |
| NM_000232.4:c.498C>T , LRG_204t1:c.498C>T | NP_000223.1:p.Ile166= | |
| XM_006714049.2:c.201C>T | XP_006714112.1:p.Ile67= | |
| XM_011534403.1:c.288C>T | XP_011532705.1:p.Ile96= | |
| XM_011534404.1:c.201C>T | XP_011532706.1:p.Ile67= | |
| NM_000232.5:c.498C>T MANE Select | NP_000223.1:p.Ile166= |