Linked Data
dbSNP Id:
rs61173206
gnomAD v2:
9-119314201-A-G
gnomAD v3:
9-116551922-A-G
gnomAD v4:
9-116551922-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.116551922A>G , CM000671.2:g.116551922A>G | GRCh38 |
| NC_000009.11:g.119314201A>G , CM000671.1:g.119314201A>G | GRCh37 |
| NC_000009.10:g.118354022A>G | NCBI36 |
| NG_021409.1:g.868117T>C | |
| NG_021409.2:g.868136T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313400.9:c.3356-64422T>C (ASTN2) MANE Select | ENSP00000314038.4:n.3356-64422T>C | |
| ENST00000361477.8:c.3203-64422T>C (ASTN2) | ENSP00000355116.5:n.3203-64422T>C | |
| ENST00000288520.9:c.659-64422T>C (ASTN2) | ENSP00000288520.5:n.659-64422T>C | |
| ENST00000313400.8:c.3356-64422T>C (ASTN2) | ENSP00000314038.4:n.3356-64422T>C | |
| ENST00000341734.8:c.512-64422T>C (ASTN2) | ENSP00000339925.4:n.512-64422T>C | |
| ENST00000361209.6:c.3203-64422T>C (ASTN2) | ENSP00000354504.2:n.3203-64422T>C | |
| ENST00000361477.7:c.512-64422T>C (ASTN2) | ENSP00000355116.4:n.512-64422T>C | |
| ENST00000373986.7:c.2525-64422T>C (ASTN2) | ENSP00000363098.3:n.2525-64422T>C | |
| NM_001184734.1:c.512-64422T>C (ASTN2) | NP_001171663.1:n.512-64422T>C | |
| NM_014010.4:c.3203-64422T>C (ASTN2) | NP_054729.3:n.3203-64422T>C | |
| NM_198186.3:c.659-64422T>C (ASTN2) | NP_937829.3:n.659-64422T>C | |
| NM_198187.3:c.512-64422T>C (ASTN2) | NP_937830.3:n.512-64422T>C | |
| NM_198188.2:c.512-64422T>C (ASTN2) | NP_937831.1:n.512-64422T>C | |
| NR_033973.1:n.1325-188A>G (ASTN2-AS1) | ||
| NM_001365068.1:c.3356-64422T>C (ASTN2) MANE Select | NP_001351997.1:n.3356-64422T>C | |
| NM_001365069.1:c.3344-64422T>C (ASTN2) | NP_001351998.1:n.3344-64422T>C | |
| NM_014010.5:c.3203-64422T>C (ASTN2) | NP_054729.3:n.3203-64422T>C |