Linked Data
dbSNP Id:
rs4792800
gnomAD v2:
17-16845167-A-G
gnomAD v3:
17-16941853-A-G
gnomAD v4:
17-16941853-A-G
Allelic Epigenome:
Alellic Epigenome (raw data)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.16941853A>G , CM000679.2:g.16941853A>G | GRCh38 |
| NC_000017.10:g.16845167A>G , CM000679.1:g.16845167A>G | GRCh37 |
| NC_000017.9:g.16785892A>G | NCBI36 |
| NG_007281.1:g.35236T>C , LRG_120:g.35236T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261652.7:c.446-1342T>C MANE Select | ENSP00000261652.2:n.446-1342T>C | |
| ENST00000261652.6:c.446-1342T>C | ENSP00000261652.2:n.446-1342T>C | |
| ENST00000579315.5:c.445+6885T>C | ENSP00000464069.1:n.445+6885T>C | |
| ENST00000581616.2:n.449-376T>C | ||
| ENST00000582931.5:n.349+6885T>C | ||
| ENST00000583789.1:c.308-1342T>C | ENSP00000462952.1:n.308-1342T>C | |
| ENST00000584950.5:c.308-1342T>C | ENSP00000463582.1:n.308-1342T>C | |
| NM_012452.2:c.446-1342T>C , LRG_120t1:c.446-1342T>C | NP_036584.1:n.446-1342T>C | |
| NM_012452.3:c.446-1342T>C MANE Select | NP_036584.1:n.446-1342T>C |