Linked Data
dbSNP Id:
rs2903692
gnomAD v2:
16-11238783-G-A
gnomAD v3:
16-11144926-G-A
gnomAD v4:
16-11144926-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11144926G>A , CM000678.2:g.11144926G>A | GRCh38 |
| NC_000016.9:g.11238783G>A , CM000678.1:g.11238783G>A | GRCh37 |
| NC_000016.8:g.11146284G>A | NCBI36 |
| NG_016757.1:g.205439G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000703130.1:c.2635+18780G>A | ENSP00000515187.1:n.2635+18780G>A | |
| ENST00000409790.6:c.2641+18780G>A MANE Select | ENSP00000387122.1:n.2641+18780G>A | |
| ENST00000261657.5:c.215+18780G>A | ||
| ENST00000409790.5:c.2641+18780G>A | ENSP00000387122.1:n.2641+18780G>A | |
| ENST00000428742.6:c.373-12151G>A | ||
| ENST00000436973.5:c.221-11648G>A | ENSP00000389963.1:n.221-11648G>A | |
| ENST00000459723.1:n.138-4960G>A | ||
| NM_015226.2:c.2641+18780G>A | NP_056041.1:n.2641+18780G>A | |
| XM_005255210.1:c.2635+18780G>A | XP_005255267.1:n.2635+18780G>A | |
| XM_005255211.1:c.2593+18780G>A | XP_005255268.1:n.2593+18780G>A | |
| XM_005255213.1:c.2587+18780G>A | XP_005255270.1:n.2587+18780G>A | |
| XM_005255214.1:c.2641+18780G>A | XP_005255271.1:n.2641+18780G>A | |
| XM_005255215.3:c.2642-11648G>A | XP_005255272.1:n.2642-11648G>A | |
| XM_005255216.1:c.2642-12151G>A | XP_005255273.1:n.2642-12151G>A | |
| XM_011522434.1:c.2512+18780G>A | XP_011520736.1:n.2512+18780G>A | |
| XM_011522435.1:c.2641+18780G>A | XP_011520737.1:n.2641+18780G>A | |
| XM_011522438.1:c.2642-4960G>A | XP_011520740.1:n.2642-4960G>A | |
| XR_932810.1:n.2865+18780G>A | ||
| XM_005255210.2:c.2635+18780G>A | XP_005255267.1:n.2635+18780G>A | |
| XM_005255211.2:c.2593+18780G>A | XP_005255268.1:n.2593+18780G>A | |
| XM_005255213.2:c.2587+18780G>A | XP_005255270.1:n.2587+18780G>A | |
| XM_005255214.2:c.2641+18780G>A | XP_005255271.1:n.2641+18780G>A | |
| XM_005255215.4:c.2642-11648G>A | XP_005255272.1:n.2642-11648G>A | |
| XM_005255216.2:c.2642-12151G>A | XP_005255273.1:n.2642-12151G>A | |
| XM_011522434.2:c.2512+18780G>A | XP_011520736.1:n.2512+18780G>A | |
| XM_011522435.2:c.2641+18780G>A | XP_011520737.1:n.2641+18780G>A | |
| XM_011522438.3:c.2642-4960G>A | XP_011520740.1:n.2642-4960G>A | |
| XM_017023090.2:c.1126+18780G>A | XP_016878579.1:n.1126+18780G>A | |
| XM_024450218.1:c.2594-11648G>A | XP_024305986.1:n.2594-11648G>A | |
| XM_024450219.1:c.1192+18780G>A | XP_024305987.1:n.1192+18780G>A | |
| XR_932810.3:n.2820+18780G>A | ||
| NM_015226.3:c.2641+18780G>A MANE Select | NP_056041.1:n.2641+18780G>A |