Linked Data
dbSNP Id:
rs1995356
gnomAD v2:
3-143029022-T-C
gnomAD v3:
3-143310180-T-C
gnomAD v4:
3-143310180-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.143310180T>C , CM000665.2:g.143310180T>C | GRCh38 |
| NC_000003.11:g.143029022T>C , CM000665.1:g.143029022T>C | GRCh37 |
| NC_000003.10:g.144511712T>C | NCBI36 |
| NG_017077.1:g.543352A>G | |
| NG_017077.2:g.543352A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000316549.11:c.1605-41200A>G MANE Select | ENSP00000320246.6:n.1605-41200A>G | |
| ENST00000316549.10:c.1605-41200A>G | ENSP00000320246.6:n.1605-41200A>G | |
| NM_173653.3:c.1605-41200A>G | NP_775924.1:n.1605-41200A>G | |
| XM_011512703.1:c.957-41200A>G | XP_011511005.1:n.957-41200A>G | |
| XM_011512703.3:c.957-41200A>G | XP_011511005.1:n.957-41200A>G | |
| XM_017006202.2:c.1712-25838A>G | XP_016861691.1:n.1712-25838A>G | |
| XM_017006203.1:c.1254-41200A>G | XP_016861692.1:n.1254-41200A>G | |
| NM_173653.4:c.1605-41200A>G MANE Select | NP_775924.1:n.1605-41200A>G |