Linked Data
dbSNP Id:
rs1887407227
gnomAD v3:
14-45159223-T-C
gnomAD v4:
14-45159223-T-C
MyVariant Identifiers:
chr14:g.45628426T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.45159223T>C , CM000676.2:g.45159223T>C | GRCh38 |
| NC_000014.8:g.45628426T>C , CM000676.1:g.45628426T>C | GRCh37 |
| NC_000014.7:g.44698176T>C | NCBI36 |
| NG_007417.1:g.28291T>C , LRG_502:g.28291T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000556036.6:c.1524T>C | ENSP00000450596.1:p.Phe508= | |
| ENST00000556250.6:c.1524T>C | ENSP00000452033.2:p.Phe508= | |
| ENST00000696641.1:c.1365T>C | ENSP00000512774.1:p.Phe455= | |
| ENST00000696642.1:c.*335T>C | ENSP00000512775.1:n.*335T>C | |
| ENST00000696643.1:c.1524T>C | ENSP00000512776.1:p.Phe508= | |
| ENST00000696646.1:c.*335T>C | ENSP00000512777.1:n.*335T>C | |
| ENST00000696647.1:c.1524T>C | ENSP00000512778.1:p.Phe508= | |
| ENST00000696648.1:c.1524T>C | ENSP00000512779.1:p.Phe508= | |
| ENST00000696649.1:c.1524T>C | ENSP00000512780.1:p.Phe508= | |
| ENST00000696650.1:n.1472T>C | ||
| ENST00000696658.1:n.2074T>C | ||
| ENST00000696662.1:c.1446T>C | ENSP00000512788.1:p.Phe482= | |
| ENST00000696663.1:c.341T>C | ||
| ENST00000696664.1:c.341T>C | ||
| ENST00000696675.1:c.1524T>C | ENSP00000512799.1:p.Phe508= | |
| ENST00000696680.1:c.1392T>C | ENSP00000512803.1:p.Phe464= | |
| ENST00000696681.1:c.*335T>C | ENSP00000512804.1:n.*335T>C | |
| ENST00000696682.1:c.1524T>C | ENSP00000512805.1:p.Phe508= | |
| ENST00000696683.1:c.341T>C | ||
| ENST00000696684.1:c.341T>C | ||
| ENST00000696685.1:c.341T>C | ||
| ENST00000267430.10:c.1524T>C MANE Select | ENSP00000267430.5:p.Phe508= | |
| ENST00000267430.9:c.1524T>C | ENSP00000267430.5:p.Phe508= | |
| ENST00000542564.6:c.1446T>C | ENSP00000442493.2:p.Phe482= | |
| ENST00000556036.5:c.1524T>C | ENSP00000450596.1:p.Phe508= | |
| ENST00000556250.5:c.279T>C | ENSP00000452033.1:p.Phe93= | |
| NM_001308133.1:c.1446T>C | NP_001295062.1:p.Phe482= | |
| NM_001308134.1:c.1524T>C | NP_001295063.1:p.Phe508= | |
| NM_020937.2:c.1524T>C , LRG_502t1:c.1524T>C | NP_065988.1:p.Phe508= | |
| NM_020937.3:c.1524T>C | NP_065988.1:p.Phe508= | |
| XM_011537034.1:c.1524T>C | XP_011535336.1:p.Phe508= | |
| XM_011537035.1:c.1446T>C | XP_011535337.1:p.Phe482= | |
| XM_011537036.1:c.1524T>C | XP_011535338.1:p.Phe508= | |
| XM_011537034.2:c.1524T>C | XP_011535336.1:p.Phe508= | |
| XM_011537035.3:c.1446T>C | XP_011535337.1:p.Phe482= | |
| XM_017021523.1:c.1524T>C | XP_016877012.1:p.Phe508= | |
| XM_017021524.2:c.561T>C | XP_016877013.1:p.Phe187= | |
| XM_017021525.2:c.339T>C | XP_016877014.1:p.Phe113= | |
| XM_017021526.2:c.339T>C | XP_016877015.1:p.Phe113= | |
| XM_017021527.1:c.339T>C | XP_016877016.1:p.Phe113= | |
| XR_001750470.1:n.1616T>C | ||
| XR_001750471.2:n.1616T>C | ||
| XR_001750472.1:n.1616T>C | ||
| NM_020937.4:c.1524T>C MANE Select | NP_065988.1:p.Phe508= | |
| NM_001308133.2:c.1446T>C | NP_001295062.1:p.Phe482= | |
| NM_001308134.2:c.1524T>C | NP_001295063.1:p.Phe508= |