Linked Data
ClinVar Variation Id:
204220
dbSNP Id:
rs2736664
ExAC:
9:37426524 C / T
gnomAD v2:
9-37426524-C-T
gnomAD v3:
9-37426527-C-T
gnomAD v4:
9-37426527-C-T
PubMed:
PMID:26484032
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.37426527C>T , CM000671.2:g.37426527C>T | GRCh38 |
| NC_000009.11:g.37426524C>T , CM000671.1:g.37426524C>T | GRCh37 |
| NC_000009.10:g.37416524C>T | NCBI36 |
| NG_008135.1:g.8818C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318158.11:c.288-11C>T MANE Select | ENSP00000313432.6:n.288-11C>T | |
| ENST00000318158.10:c.288-11C>T | ENSP00000313432.6:n.288-11C>T | |
| ENST00000377824.8:n.325-11C>T | ||
| ENST00000460882.5:n.315-11C>T | ||
| ENST00000487399.5:n.829C>T | ||
| ENST00000491488.5:n.110-1957C>T | ||
| ENST00000493368.5:n.345-11C>T | ||
| ENST00000607784.1:c.288-11C>T | ENSP00000475569.1:n.288-11C>T | |
| NM_012203.1:c.288-11C>T | NP_036335.1:n.288-11C>T | |
| XM_005251631.1:c.84-1957C>T | XP_005251688.1:n.84-1957C>T | |
| XM_011518073.1:c.-475-11C>T | XP_011516375.1:n.-475-11C>T | |
| XR_929374.1:n.373-11C>T | ||
| XM_017015320.2:c.288-11C>T | XP_016870809.1:n.288-11C>T | |
| XM_017015321.2:c.288-11C>T | XP_016870810.1:n.288-11C>T | |
| XM_017015323.2:c.-475-11C>T | XP_016870812.1:n.-475-11C>T | |
| XM_024447716.1:c.561-11C>T | XP_024303484.1:n.561-11C>T | |
| XM_024447717.1:c.561-11C>T | XP_024303485.1:n.561-11C>T | |
| XR_002956828.1:n.576-11C>T | ||
| XR_002956829.1:n.576-11C>T | ||
| XR_002956830.1:n.347-11C>T | ||
| XR_002956831.1:n.139-1957C>T | ||
| XR_002956832.1:n.347-11C>T | ||
| NM_012203.2:c.288-11C>T MANE Select | NP_036335.1:n.288-11C>T |