Linked Data
ClinVar Variation Id:
360920
dbSNP Id:
rs370536529
ExAC:
7:92129015 T / C
gnomAD v2:
7-92129015-T-C
gnomAD v3:
7-92499701-T-C
gnomAD v4:
7-92499701-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92499701T>C , CM000669.2:g.92499701T>C | GRCh38 |
| NC_000007.13:g.92129015T>C , CM000669.1:g.92129015T>C | GRCh37 |
| NC_000007.12:g.91966951T>C | NCBI36 |
| NG_008341.1:g.33831A>G | |
| NG_008341.2:g.33831A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000248633.9:c.2718+3A>G MANE Select | ENSP00000248633.4:n.2718+3A>G | |
| ENST00000248633.8:c.2718+3A>G | ENSP00000248633.4:n.2718+3A>G | |
| ENST00000428214.5:c.2547+3A>G | ENSP00000394413.1:n.2547+3A>G | |
| ENST00000438045.5:c.1752+3A>G | ENSP00000410438.1:n.1752+3A>G | |
| ENST00000484913.5:n.2757+3A>G | ||
| ENST00000496420.5:n.2610+3A>G | ||
| NM_000466.2:c.2718+3A>G | NP_000457.1:n.2718+3A>G | |
| NM_001282677.1:c.2547+3A>G | NP_001269606.1:n.2547+3A>G | |
| NM_001282678.1:c.2094+3A>G | NP_001269607.1:n.2094+3A>G | |
| XM_005250433.3:c.969+3A>G | XP_005250490.1:n.969+3A>G | |
| XR_242246.3:n.2814+3A>G | ||
| XM_017012319.2:c.969+3A>G | XP_016867808.1:n.969+3A>G | |
| XR_001744808.2:n.1745+3A>G | ||
| XR_242246.5:n.2765+3A>G | ||
| NM_000466.3:c.2718+3A>G MANE Select | NP_000457.1:n.2718+3A>G | |
| NM_001282677.2:c.2547+3A>G | NP_001269606.1:n.2547+3A>G | |
| NM_001282678.2:c.2094+3A>G | NP_001269607.1:n.2094+3A>G |