Linked Data
ClinVar Variation Id:
1107371
ClinVar RCV Id:
RCV001432478
dbSNP Id:
rs2142382363
MyVariant Identifiers:
chr16:g.23641423G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23630102G>A , CM000678.2:g.23630102G>A | GRCh38 |
| NC_000016.9:g.23641423G>A , CM000678.1:g.23641423G>A | GRCh37 |
| NC_000016.8:g.23548924G>A | NCBI36 |
| NG_007406.1:g.16256C>T , LRG_308:g.16256C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.2058C>T | ENSP00000460666.3:p.Pro686= | |
| ENST00000565038.2:c.212-827C>T | ENSP00000459882.2:n.212-827C>T | |
| ENST00000566069.6:c.2052C>T | ENSP00000459237.2:p.Pro684= | |
| ENST00000697377.2:c.2058C>T | ENSP00000513286.2:p.Pro686= | |
| ENST00000697379.2:c.2058C>T | ENSP00000513287.2:p.Pro686= | |
| ENST00000561514.2:c.1167C>T | ENSP00000460666.2:p.Pro389= | |
| ENST00000697374.1:c.1167C>T | ENSP00000513284.1:p.Pro389= | |
| ENST00000697375.1:n.3399C>T | ||
| ENST00000697376.1:c.1167C>T | ENSP00000513285.1:p.Pro389= | |
| ENST00000697377.1:c.1167C>T | ENSP00000513286.1:p.Pro389= | |
| ENST00000697378.1:n.2572C>T | ||
| ENST00000697379.1:c.1167C>T | ENSP00000513287.1:p.Pro389= | |
| ENST00000697380.1:n.980C>T | ||
| ENST00000697381.1:n.747C>T | ||
| ENST00000697382.1:c.1167C>T | ENSP00000513288.1:p.Pro389= | |
| ENST00000697383.1:c.49-827C>T | ENSP00000513289.1:n.49-827C>T | |
| ENST00000697384.1:n.2206C>T | ||
| ENST00000261584.9:c.2052C>T MANE Select | ENSP00000261584.4:p.Pro684= | |
| ENST00000261584.8:c.2052C>T | ENSP00000261584.4:p.Pro684= | |
| ENST00000565038.1:c.87-827C>T | ||
| ENST00000568219.5:c.1167C>T | ENSP00000454703.2:p.Pro389= | |
| NM_024675.3:c.2052C>T , LRG_308t1:c.2052C>T | NP_078951.2:p.Pro684= | |
| XM_011545946.1:c.2058C>T | XP_011544248.1:p.Pro686= | |
| XM_011545947.1:c.2058C>T | XP_011544249.1:p.Pro686= | |
| XM_011545948.1:c.1167C>T | XP_011544250.1:p.Pro389= | |
| XR_950851.1:n.2848C>T | ||
| XM_011545946.2:c.2058C>T | XP_011544248.1:p.Pro686= | |
| XM_011545947.2:c.2058C>T | XP_011544249.1:p.Pro686= | |
| XM_011545948.2:c.1167C>T | XP_011544250.1:p.Pro389= | |
| XM_017023671.1:c.2058C>T | XP_016879160.1:p.Pro686= | |
| XM_017023672.2:c.2052C>T | XP_016879161.1:p.Pro684= | |
| XM_017023673.2:c.2052C>T | XP_016879162.1:p.Pro684= | |
| NM_024675.4:c.2052C>T MANE Select | NP_078951.2:p.Pro684= |