Linked Data
ClinVar Variation Id:
1102582
ClinVar RCV Id:
RCV001425928
dbSNP Id:
rs1326656501
gnomAD v4:
4-80202413-G-C
MyVariant Identifiers:
chr4:g.81123567G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.80202413G>C , CM000666.2:g.80202413G>C | GRCh38 |
| NC_000004.11:g.81123567G>C , CM000666.1:g.81123567G>C | GRCh37 |
| NC_000004.10:g.81342591G>C | NCBI36 |
| NG_046725.1:g.22144G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415738.3:c.951G>C MANE Select | ENSP00000406998.2:p.Pro317= | |
| ENST00000339711.8:c.951G>C | ENSP00000339764.4:p.Pro317= | |
| ENST00000415738.2:c.951G>C | ENSP00000406998.2:p.Pro317= | |
| ENST00000504452.5:c.951G>C | ENSP00000423985.1:p.Pro317= | |
| ENST00000515013.5:c.951G>C | ENSP00000425149.1:p.Pro317= | |
| NM_001099403.1:c.951G>C | NP_001092873.1:p.Pro317= | |
| NM_020226.3:c.951G>C | NP_064611.3:p.Pro317= | |
| XM_005263144.2:c.954G>C | XP_005263201.1:p.Pro318= | |
| XM_005263145.2:c.954G>C | XP_005263202.1:p.Pro318= | |
| XM_005263146.3:c.951G>C | XP_005263203.1:p.Pro317= | |
| XM_011532133.1:c.1794G>C | XP_011530435.1:p.Pro598= | |
| XM_011532134.1:c.1791G>C | XP_011530436.1:p.Pro597= | |
| XM_011532135.1:c.1653G>C | XP_011530437.1:p.Pro551= | |
| XM_011532136.1:c.1506G>C | XP_011530438.1:p.Pro502= | |
| XM_011532137.1:c.1506G>C | XP_011530439.1:p.Pro502= | |
| XM_011532138.1:c.1506G>C | XP_011530440.1:p.Pro502= | |
| XM_011532139.1:c.1506G>C | XP_011530441.1:p.Pro502= | |
| XM_011532140.1:c.1506G>C | XP_011530442.1:p.Pro502= | |
| XM_011532141.1:c.1368G>C | XP_011530443.1:p.Pro456= | |
| XM_011532142.1:c.1347G>C | XP_011530444.1:p.Pro449= | |
| XM_005263146.4:c.951G>C | XP_005263203.1:p.Pro317= | |
| XM_011532133.2:c.1794G>C | XP_011530435.1:p.Pro598= | |
| XM_011532135.2:c.1653G>C | XP_011530437.1:p.Pro551= | |
| XM_011532140.2:c.1506G>C | XP_011530442.1:p.Pro502= | |
| XM_011532141.3:c.1368G>C | XP_011530443.1:p.Pro456= | |
| XM_017008468.1:c.1503G>C | XP_016863957.1:p.Pro501= | |
| XM_017008469.1:c.1590G>C | XP_016863958.1:p.Pro530= | |
| XM_017008470.1:c.1506G>C | XP_016863959.1:p.Pro502= | |
| NM_001099403.2:c.951G>C MANE Select | NP_001092873.1:p.Pro317= | |
| NM_020226.4:c.951G>C | NP_064611.3:p.Pro317= |