Linked Data
dbSNP Id:
rs747491224
ExAC:
14:91739062 G / C
gnomAD v2:
14-91739062-G-C
gnomAD v3:
14-91272718-G-C
gnomAD v4:
14-91272718-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272718G>C , CM000676.2:g.91272718G>C | GRCh38 |
| NC_000014.8:g.91739062G>C , CM000676.1:g.91739062G>C | GRCh37 |
| NC_000014.7:g.90808815G>C | NCBI36 |
| NG_033118.1:g.150127C>G | |
| NG_033118.2:g.150127C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5994C>G MANE Select | ENSP00000374507.6:p.Asp1998Glu | |
| ENST00000331194.8:c.1428C>G | ENSP00000330332.8:p.Asp476Glu | |
| ENST00000389857.10:c.5994C>G | ENSP00000374507.6:p.Asp1998Glu | |
| ENST00000556726.5:c.2222C>G | ||
| NM_001080414.3:c.5994C>G | NP_001073883.2:p.Asp1998Glu | |
| XM_011536796.1:c.5886C>G | XP_011535098.1:p.Asp1962Glu | |
| XM_011536796.2:c.5886C>G | XP_011535098.1:p.Asp1962Glu | |
| XM_017021336.1:c.3075C>G | XP_016876825.1:p.Asp1025Glu | |
| NM_001080414.4:c.5994C>G MANE Select | NP_001073883.2:p.Asp1998Glu |