Linked Data
ClinVar Variation Id:
197696
dbSNP Id:
rs144455258
ExAC:
2:219677693 G / T
gnomAD v2:
2-219677693-G-T
gnomAD v3:
2-218812970-G-T
gnomAD v4:
2-218812970-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812970G>T , CM000664.2:g.218812970G>T | GRCh38 |
| NC_000002.11:g.219677693G>T , CM000664.1:g.219677693G>T | GRCh37 |
| NC_000002.10:g.219385937G>T | NCBI36 |
| NG_007959.1:g.36222G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.891G>T MANE Select | ENSP00000258415.4:p.Leu297= | |
| ENST00000258415.8:c.891G>T | ENSP00000258415.4:p.Leu297= | |
| ENST00000411688.1:c.609G>T | ENSP00000392671.1:p.Leu203= | |
| ENST00000445971.1:c.*352G>T | ENSP00000404945.1:n.*352G>T | |
| ENST00000466602.1:n.1013G>T | ||
| ENST00000494263.5:n.1325G>T | ||
| NM_000784.3:c.891G>T | NP_000775.1:p.Leu297= | |
| XM_017003488.2:c.471G>T | XP_016858977.1:p.Leu157= | |
| NM_000784.4:c.891G>T MANE Select | NP_000775.1:p.Leu297= |