Linked Data
dbSNP Id:
rs1881438706
gnomAD v4:
14-20457190-G-A
MyVariant Identifiers:
chr14:g.20925349G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.20457190G>A , CM000676.2:g.20457190G>A | GRCh38 |
| NC_000014.8:g.20925349G>A , CM000676.1:g.20925349G>A | GRCh37 |
| NC_000014.7:g.19995189G>A | NCBI36 |
| NG_008718.1:g.7060G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216714.8:c.639G>A MANE Select | ENSP00000216714.3:p.Val213= | |
| ENST00000216714.7:c.639G>A | ENSP00000216714.3:p.Val213= | |
| ENST00000398030.8:c.639G>A | ENSP00000381111.4:p.Val213= | |
| ENST00000438886.1:c.419G>A | ||
| ENST00000553555.5:n.1059G>A | ||
| ENST00000553681.5:c.639G>A | ENSP00000451327.1:p.Val213= | |
| ENST00000555414.5:c.639G>A | ENSP00000451979.1:p.Val213= | |
| ENST00000555839.5:c.552G>A | ENSP00000452460.1:p.Val184= | |
| ENST00000557054.1:c.*50G>A | ENSP00000452212.2:n.*50G>A | |
| ENST00000557159.5:n.1255G>A | ||
| ENST00000557365.1:n.719G>A | ||
| NM_001244249.1:c.639G>A | NP_001231178.1:p.Val213= | |
| NM_001641.3:c.639G>A | NP_001632.2:p.Val213= | |
| NM_080648.2:c.639G>A | NP_542379.1:p.Val213= | |
| NM_080649.2:c.639G>A | NP_542380.1:p.Val213= | |
| XM_005267581.3:c.639G>A | XP_005267638.1:p.Val213= | |
| XM_005267582.3:c.588G>A | XP_005267639.1:p.Val196= | |
| NM_001641.4:c.639G>A MANE Select | NP_001632.2:p.Val213= | |
| NM_001244249.2:c.639G>A | NP_001231178.1:p.Val213= | |
| NM_080648.3:c.639G>A | NP_542379.1:p.Val213= | |
| NM_080649.3:c.639G>A | NP_542380.1:p.Val213= |