Linked Data
dbSNP Id:
rs776035497
ExAC:
7:92123968 T / C
gnomAD v2:
7-92123968-T-C
gnomAD v3:
7-92494654-T-C
gnomAD v4:
7-92494654-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92494654T>C , CM000669.2:g.92494654T>C | GRCh38 |
| NC_000007.13:g.92123968T>C , CM000669.1:g.92123968T>C | GRCh37 |
| NC_000007.12:g.91961904T>C | NCBI36 |
| NG_008341.1:g.38878A>G | |
| NG_008341.2:g.38878A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.2784-25A>G MANE Select | ENSP00000248633.4:n.2784-25A>G | |
| ENST00000248633.8:c.2784-25A>G | ENSP00000248633.4:n.2784-25A>G | |
| ENST00000428214.5:c.2613-25A>G | ENSP00000394413.1:n.2613-25A>G | |
| ENST00000438045.5:c.1818-25A>G | ENSP00000410438.1:n.1818-25A>G | |
| ENST00000484913.5:n.2823-25A>G | ||
| ENST00000496420.5:n.2676-25A>G | ||
| NM_000466.2:c.2784-25A>G | NP_000457.1:n.2784-25A>G | |
| NM_001282677.1:c.2613-25A>G | NP_001269606.1:n.2613-25A>G | |
| NM_001282678.1:c.2160-25A>G | NP_001269607.1:n.2160-25A>G | |
| XM_005250433.3:c.1035-25A>G | XP_005250490.1:n.1035-25A>G | |
| XR_242246.3:n.2880-25A>G | ||
| XM_017012319.2:c.1035-25A>G | XP_016867808.1:n.1035-25A>G | |
| XR_001744808.2:n.1811-25A>G | ||
| XR_242246.5:n.2831-25A>G | ||
| NM_000466.3:c.2784-25A>G MANE Select | NP_000457.1:n.2784-25A>G | |
| NM_001282677.2:c.2613-25A>G | NP_001269606.1:n.2613-25A>G | |
| NM_001282678.2:c.2160-25A>G | NP_001269607.1:n.2160-25A>G |