Linked Data
ClinVar Variation Id:
492140
ClinVar RCV Id:
RCV000583508
dbSNP Id:
rs1038099508
gnomAD v2:
16-23652488-G-A
gnomAD v3:
16-23641167-G-A
gnomAD v4:
16-23641167-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23641167G>A , CM000678.2:g.23641167G>A | GRCh38 |
| NC_000016.9:g.23652488G>A , CM000678.1:g.23652488G>A | GRCh37 |
| NC_000016.8:g.23559989G>A | NCBI36 |
| NG_007406.1:g.5191C>T , LRG_308:g.5191C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000561514.3:c.-862C>T | ENSP00000460666.3:n.-862C>T | |
| ENST00000565038.2:c.-10C>T | ENSP00000459882.2:n.-10C>T | |
| ENST00000566069.6:c.-10C>T | ENSP00000459237.2:n.-10C>T | |
| ENST00000697377.2:c.-249C>T | ENSP00000513286.2:n.-249C>T | |
| ENST00000697379.2:c.-155C>T | ENSP00000513287.2:n.-155C>T | |
| ENST00000561514.2:c.-1753C>T | ENSP00000460666.2:n.-1753C>T | |
| ENST00000697374.1:c.-1344C>T | ENSP00000513284.1:n.-1344C>T | |
| ENST00000697376.1:c.-1065C>T | ENSP00000513285.1:n.-1065C>T | |
| ENST00000697377.1:c.-1140C>T | ENSP00000513286.1:n.-1140C>T | |
| ENST00000697379.1:c.-1046C>T | ENSP00000513287.1:n.-1046C>T | |
| ENST00000697382.1:c.-1804C>T | ENSP00000513288.1:n.-1804C>T | |
| ENST00000697383.1:c.-10C>T | ENSP00000513289.1:n.-10C>T | |
| ENST00000697384.1:n.145C>T | ||
| ENST00000261584.9:c.-10C>T MANE Select | ENSP00000261584.4:n.-10C>T | |
| ENST00000261584.8:c.-10C>T | ENSP00000261584.4:n.-10C>T | |
| ENST00000567003.1:n.135C>T | ||
| ENST00000568219.5:c.-878C>T | ENSP00000454703.2:n.-878C>T | |
| NM_024675.3:c.-10C>T , LRG_308t1:c.-10C>T | NP_078951.2:n.-10C>T | |
| XM_011545948.1:c.-1029C>T | XP_011544250.1:n.-1029C>T | |
| XM_011545946.2:c.-862C>T | XP_011544248.1:n.-862C>T | |
| XM_011545947.2:c.-862C>T | XP_011544249.1:n.-862C>T | |
| XM_011545948.2:c.-1029C>T | XP_011544250.1:n.-1029C>T | |
| XM_017023671.1:c.-862C>T | XP_016879160.1:n.-862C>T | |
| XM_017023672.2:c.-10C>T | XP_016879161.1:n.-10C>T | |
| XM_017023673.2:c.-10C>T | XP_016879162.1:n.-10C>T | |
| NM_024675.4:c.-10C>T MANE Select | NP_078951.2:n.-10C>T |