Linked Data
ClinVar Variation Id:
1582423
ClinVar RCV Id:
RCV002097493
dbSNP Id:
rs762582964
ExAC:
7:92126110 G / C
gnomAD v2:
7-92126110-G-C
gnomAD v3:
7-92496796-G-C
gnomAD v4:
7-92496796-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92496796G>C , CM000669.2:g.92496796G>C | GRCh38 |
| NC_000007.13:g.92126110G>C , CM000669.1:g.92126110G>C | GRCh37 |
| NC_000007.12:g.91964046G>C | NCBI36 |
| NG_008341.1:g.36736C>G | |
| NG_008341.2:g.36736C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000248633.9:c.2719-19C>G MANE Select | ENSP00000248633.4:n.2719-19C>G | |
| ENST00000248633.8:c.2719-19C>G | ENSP00000248633.4:n.2719-19C>G | |
| ENST00000428214.5:c.2548-19C>G | ENSP00000394413.1:n.2548-19C>G | |
| ENST00000438045.5:c.1753-19C>G | ENSP00000410438.1:n.1753-19C>G | |
| ENST00000484913.5:n.2758-19C>G | ||
| ENST00000496420.5:n.2611-19C>G | ||
| NM_000466.2:c.2719-19C>G | NP_000457.1:n.2719-19C>G | |
| NM_001282677.1:c.2548-19C>G | NP_001269606.1:n.2548-19C>G | |
| NM_001282678.1:c.2095-19C>G | NP_001269607.1:n.2095-19C>G | |
| XM_005250433.3:c.970-19C>G | XP_005250490.1:n.970-19C>G | |
| XR_242246.3:n.2815-19C>G | ||
| XM_017012319.2:c.970-19C>G | XP_016867808.1:n.970-19C>G | |
| XR_001744808.2:n.1746-19C>G | ||
| XR_242246.5:n.2766-19C>G | ||
| NM_000466.3:c.2719-19C>G MANE Select | NP_000457.1:n.2719-19C>G | |
| NM_001282677.2:c.2548-19C>G | NP_001269606.1:n.2548-19C>G | |
| NM_001282678.2:c.2095-19C>G | NP_001269607.1:n.2095-19C>G |