Linked Data
dbSNP Id:
rs1444916210
gnomAD v3:
12-7086238-G-A
gnomAD v4:
12-7086238-G-A
MyVariant Identifiers:
chr12:g.7086238G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7086238G>A , CM000674.2:g.7086238G>A | GRCh38 |
| NG_062465.1:g.11370C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647956.2:c.1117+141C>T MANE Select | ENSP00000497341.1:n.1117+141C>T | |
| ENST00000648162.1:n.1089+141C>T | ||
| ENST00000649804.1:c.211+141C>T | ENSP00000497938.1:n.211+141C>T | |
| ENST00000535233.6:c.1015+141C>T | ENSP00000438636.3:n.1015+141C>T | |
| ENST00000536053.6:c.1159+141C>T | ENSP00000444271.3:n.1159+141C>T | |
| ENST00000540394.5:n.2182+141C>T | ||
| ENST00000542285.5:c.1117+141C>T | ENSP00000438615.2:n.1117+141C>T | |
| ENST00000602298.2:n.1466+141C>T | ||
| NM_001733.4:c.1117+141C>T | NP_001724.3:n.1117+141C>T | |
| NM_001354346.1:c.1159+141C>T | NP_001341275.1:n.1159+141C>T | |
| NM_001733.6:c.1117+141C>T | NP_001724.4:n.1117+141C>T | |
| NM_001733.7:c.1117+141C>T MANE Select | NP_001724.4:n.1117+141C>T | |
| NM_001354346.2:c.1159+141C>T | NP_001341275.1:n.1159+141C>T |