Linked Data
ClinVar Variation Id:
947202
ClinVar RCV Id:
RCV001218224
dbSNP Id:
rs2069743547
gnomAD v4:
17-31338729-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.31338729C>T , CM000679.2:g.31338729C>T | GRCh38 |
| NC_000017.10:g.29665747C>T , CM000679.1:g.29665747C>T | GRCh37 |
| NC_000017.9:g.26689873C>T | NCBI36 |
| NG_009018.1:g.248753C>T , LRG_214:g.248753C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696138.1:c.6827C>T | ENSP00000512431.1:p.Pro2276Leu | |
| ENST00000684826.1:c.1409C>T | ENSP00000509994.1:p.Pro470Leu | |
| ENST00000684998.1:n.2667C>T | ||
| ENST00000687027.1:c.1001C>T | ENSP00000508715.1:p.Pro334Leu | |
| ENST00000687863.1:n.3490C>T | ||
| ENST00000691014.1:c.6875C>T | ENSP00000510595.1:p.Pro2292Leu | |
| ENST00000693617.1:c.1409C>T | ENSP00000510031.1:p.Pro470Leu | |
| ENST00000358273.9:c.6845C>T MANE Select | ENSP00000351015.4:p.Pro2282Leu | |
| ENST00000356175.7:c.6782C>T | ENSP00000348498.3:p.Pro2261Leu | |
| ENST00000358273.8:c.6845C>T | ENSP00000351015.4:p.Pro2282Leu | |
| ENST00000456735.6:c.5780C>T | ENSP00000389907.2:p.Pro1927Leu | |
| ENST00000471572.6:c.228C>T | ||
| ENST00000579081.5:c.6981C>T | ENSP00000462408.1:n.6981C>T | |
| ENST00000581790.5:c.64+849C>T | ||
| ENST00000584328.1:n.259C>T | ||
| NM_000267.3:c.6782C>T , LRG_214t1:c.6782C>T | NP_000258.1:p.Pro2261Leu | |
| NM_001042492.2:c.6845C>T , LRG_214t2:c.6845C>T | NP_001035957.1:p.Pro2282Leu | |
| XM_005257983.1:c.6845C>T | XP_005258040.1:p.Pro2282Leu | |
| XM_005257984.1:c.6782C>T | XP_005258041.1:p.Pro2261Leu | |
| XM_006721922.1:c.6875C>T | XP_006721985.1:p.Pro2292Leu | |
| XM_006721923.2:c.6836C>T | XP_006721986.1:p.Pro2279Leu | |
| XM_006721924.1:c.6875C>T | XP_006721987.1:p.Pro2292Leu | |
| XM_006721925.1:c.6812C>T | XP_006721988.1:p.Pro2271Leu | |
| XM_006721926.2:c.6875C>T | XP_006721989.1:p.Pro2292Leu | |
| XM_006721927.1:c.6875C>T | XP_006721990.1:p.Pro2292Leu | |
| XM_011524852.1:c.6872C>T | XP_011523154.1:p.Pro2291Leu | |
| XM_011524853.1:c.6836C>T | XP_011523155.1:p.Pro2279Leu | |
| XM_011524854.1:c.6836C>T | XP_011523156.1:p.Pro2279Leu | |
| XM_011524855.1:c.6836C>T | XP_011523157.1:p.Pro2279Leu | |
| XM_011524856.1:c.6836C>T | XP_011523158.1:p.Pro2279Leu | |
| XM_011524857.1:c.6875C>T | XP_011523159.1:p.Pro2292Leu | |
| NM_001042492.3:c.6845C>T MANE Select | NP_001035957.1:p.Pro2282Leu |