Linked Data
ClinVar Variation Id:
281017
dbSNP Id:
rs374999809
ExAC:
12:103271325 G / A
gnomAD v2:
12-103271325-G-A
gnomAD v3:
12-102877547-G-A
gnomAD v4:
12-102877547-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102877547G>A , CM000674.2:g.102877547G>A | GRCh38 |
| NC_000012.11:g.103271325G>A , CM000674.1:g.103271325G>A | GRCh37 |
| NC_000012.10:g.101795455G>A | NCBI36 |
| NG_008690.1:g.45056C>T | |
| NG_008690.2:g.85864C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.356C>T MANE Select | ENSP00000448059.1:p.Pro119Leu | |
| ENST00000307000.7:c.341C>T | ENSP00000303500.2:p.Pro114Leu | |
| ENST00000549111.5:n.452C>T | ||
| ENST00000550978.6:c.340C>T | ||
| ENST00000551337.5:c.356C>T | ENSP00000447620.1:p.Pro119Leu | |
| ENST00000551988.5:n.445C>T | ||
| ENST00000553106.5:c.356C>T | ENSP00000448059.1:p.Pro119Leu | |
| NM_000277.1:c.356C>T | NP_000268.1:p.Pro119Leu | |
| XM_011538422.1:c.356C>T | XP_011536724.1:p.Pro119Leu | |
| NM_000277.2:c.356C>T | NP_000268.1:p.Pro119Leu | |
| NM_001354304.1:c.356C>T | NP_001341233.1:p.Pro119Leu | |
| XM_017019370.2:c.356C>T | XP_016874859.1:p.Pro119Leu | |
| NM_000277.3:c.356C>T MANE Select | NP_000268.1:p.Pro119Leu | |
| NM_001354304.2:c.356C>T | NP_001341233.1:p.Pro119Leu |