Linked Data
ClinVar Variation Id:
137597
dbSNP Id:
rs3212752
ExAC:
19:17948732 T / C
gnomAD v2:
19-17948732-T-C
gnomAD v3:
19-17837923-T-C
gnomAD v4:
19-17837923-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.17837923T>C , CM000681.2:g.17837923T>C | GRCh38 |
| NC_000019.9:g.17948732T>C , CM000681.1:g.17948732T>C | GRCh37 |
| NC_000019.8:g.17809732T>C | NCBI36 |
| NG_007273.1:g.15069A>G , LRG_77:g.15069A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000526008.6:c.*258+9A>G | ENSP00000513006.1:n.*258+9A>G | |
| ENST00000696967.1:n.878+9A>G | ||
| ENST00000696970.1:n.356+9A>G | ||
| ENST00000458235.7:c.1701+9A>G MANE Select | ENSP00000391676.1:n.1701+9A>G | |
| ENST00000458235.5:c.1701+9A>G | ENSP00000391676.1:n.1701+9A>G | |
| ENST00000527031.5:n.1791+9A>G | ||
| ENST00000527670.5:c.1701+9A>G | ENSP00000432511.1:n.1701+9A>G | |
| ENST00000534444.1:c.1701+9A>G | ENSP00000436421.1:n.1701+9A>G | |
| NM_000215.3:c.1701+9A>G , LRG_77t1:c.1701+9A>G | NP_000206.2:n.1701+9A>G | |
| XM_005259896.2:c.1830+9A>G | XP_005259953.1:n.1830+9A>G | |
| XM_006722745.2:c.1701+9A>G | XP_006722808.1:n.1701+9A>G | |
| XM_011527990.1:c.1830+9A>G | XP_011526292.1:n.1830+9A>G | |
| XM_011527991.1:c.1830+9A>G | XP_011526293.1:n.1830+9A>G | |
| XR_430137.2:n.1840+9A>G | ||
| XM_005259896.3:c.1830+9A>G | XP_005259953.1:n.1830+9A>G | |
| XM_011527991.2:c.1830+9A>G | XP_011526293.1:n.1830+9A>G | |
| NM_000215.4:c.1701+9A>G MANE Select | NP_000206.2:n.1701+9A>G |