Linked Data
ClinVar Variation Id:
1644125
ClinVar RCV Id:
RCV002138743
dbSNP Id:
rs370111724
ExAC:
10:26243950 G / C
gnomAD v2:
10-26243950-G-C
gnomAD v3:
10-25955021-G-C
gnomAD v4:
10-25955021-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.25955021G>C , CM000672.2:g.25955021G>C | GRCh38 |
| NC_000010.10:g.26243950G>C , CM000672.1:g.26243950G>C | GRCh37 |
| NC_000010.9:g.26283956G>C | NCBI36 |
| NG_011635.1:g.25949G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376301.2:n.314+13G>C | ||
| ENST00000642197.1:n.507+13G>C | ||
| ENST00000642920.2:c.303+13G>C MANE Select | ENSP00000495965.1:n.303+13G>C | |
| ENST00000647478.1:c.303+13G>C | ENSP00000493932.1:n.303+13G>C | |
| ENST00000265944.9:c.303+13G>C | ENSP00000265944.4:n.303+13G>C | |
| ENST00000376301.1:c.303+13G>C | ENSP00000365478.1:n.303+13G>C | |
| ENST00000376302.5:c.303+13G>C | ENSP00000365479.1:n.303+13G>C | |
| ENST00000543632.5:c.303+13G>C | ENSP00000445909.1:n.303+13G>C | |
| NM_017433.4:c.303+13G>C | NP_059129.3:n.303+13G>C | |
| XM_011519498.1:c.303+13G>C | XP_011517800.1:n.303+13G>C | |
| XM_011519499.1:c.303+13G>C | XP_011517801.1:n.303+13G>C | |
| XM_011519500.1:c.303+13G>C | XP_011517802.1:n.303+13G>C | |
| XM_011519501.1:c.303+13G>C | XP_011517803.1:n.303+13G>C | |
| XM_011519502.1:c.303+13G>C | XP_011517804.1:n.303+13G>C | |
| XM_011519503.1:c.303+13G>C | XP_011517805.1:n.303+13G>C | |
| XM_011519504.1:c.303+13G>C | XP_011517806.1:n.303+13G>C | |
| XM_011519505.1:c.303+13G>C | XP_011517807.1:n.303+13G>C | |
| XM_011519506.1:c.303+13G>C | XP_011517808.1:n.303+13G>C | |
| XM_011519508.1:c.303+13G>C | XP_011517810.1:n.303+13G>C | |
| XM_011519509.1:c.303+13G>C | XP_011517811.1:n.303+13G>C | |
| XM_011519510.1:c.303+13G>C | XP_011517812.1:n.303+13G>C | |
| XM_011519511.1:c.303+13G>C | XP_011517813.1:n.303+13G>C | |
| XR_930492.1:n.507+13G>C | ||
| XR_930493.1:n.507+13G>C | ||
| XR_930494.1:n.507+13G>C | ||
| XM_011519498.2:c.303+13G>C | XP_011517800.1:n.303+13G>C | |
| XM_011519500.2:c.303+13G>C | XP_011517802.1:n.303+13G>C | |
| XM_011519506.2:c.303+13G>C | XP_011517808.1:n.303+13G>C | |
| XM_011519508.2:c.303+13G>C | XP_011517810.1:n.303+13G>C | |
| XM_011519510.2:c.303+13G>C | XP_011517812.1:n.303+13G>C | |
| XM_011519511.2:c.303+13G>C | XP_011517813.1:n.303+13G>C | |
| XR_001747111.1:n.507+13G>C | ||
| NM_017433.5:c.303+13G>C MANE Select | NP_059129.3:n.303+13G>C | |
| NM_001368265.1:c.303+13G>C | NP_001355194.1:n.303+13G>C |