Linked Data
dbSNP Id:
rs1276669765
gnomAD v2:
17-16845036-T-C
gnomAD v3:
17-16941722-T-C
gnomAD v4:
17-16941722-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.16941722T>C , CM000679.2:g.16941722T>C | GRCh38 |
| NC_000017.10:g.16845036T>C , CM000679.1:g.16845036T>C | GRCh37 |
| NC_000017.9:g.16785761T>C | NCBI36 |
| NG_007281.1:g.35367A>G , LRG_120:g.35367A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261652.7:c.446-1211A>G MANE Select | ENSP00000261652.2:n.446-1211A>G | |
| ENST00000261652.6:c.446-1211A>G | ENSP00000261652.2:n.446-1211A>G | |
| ENST00000579315.5:c.445+7016A>G | ENSP00000464069.1:n.445+7016A>G | |
| ENST00000581616.2:n.449-245A>G | ||
| ENST00000582931.5:n.349+7016A>G | ||
| ENST00000583789.1:c.308-1211A>G | ENSP00000462952.1:n.308-1211A>G | |
| ENST00000584950.5:c.308-1211A>G | ENSP00000463582.1:n.308-1211A>G | |
| NM_012452.2:c.446-1211A>G , LRG_120t1:c.446-1211A>G | NP_036584.1:n.446-1211A>G | |
| NM_012452.3:c.446-1211A>G MANE Select | NP_036584.1:n.446-1211A>G |