Linked Data
ClinVar Variation Id:
1367370
ClinVar RCV Id:
RCV001947264
dbSNP Id:
rs1341957716
gnomAD v4:
7-92517538-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92517538G>A , CM000669.2:g.92517538G>A | GRCh38 |
| NC_000007.13:g.92146852G>A , CM000669.1:g.92146852G>A | GRCh37 |
| NC_000007.12:g.91984788G>A | NCBI36 |
| NG_008341.1:g.15994C>T | |
| NG_008341.2:g.15994C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.977C>T MANE Select | ENSP00000248633.4:p.Pro326Leu | |
| ENST00000248633.8:c.977C>T | ENSP00000248633.4:p.Pro326Leu | |
| ENST00000428214.5:c.977C>T | ENSP00000394413.1:p.Pro326Leu | |
| ENST00000438045.5:c.274-3571C>T | ENSP00000410438.1:n.274-3571C>T | |
| ENST00000484913.5:n.1016C>T | ||
| NM_000466.2:c.977C>T | NP_000457.1:p.Pro326Leu | |
| NM_001282677.1:c.977C>T | NP_001269606.1:p.Pro326Leu | |
| NM_001282678.1:c.353C>T | NP_001269607.1:p.Pro118Leu | |
| XR_242246.3:n.1073C>T | ||
| XM_017012319.2:c.-690C>T | XP_016867808.1:n.-690C>T | |
| XR_001744808.2:n.87C>T | ||
| XR_242246.5:n.1024C>T | ||
| NM_000466.3:c.977C>T MANE Select | NP_000457.1:p.Pro326Leu | |
| NM_001282677.2:c.977C>T | NP_001269606.1:p.Pro326Leu | |
| NM_001282678.2:c.353C>T | NP_001269607.1:p.Pro118Leu |