Linked Data
ClinVar Variation Id:
292845
dbSNP Id:
rs56271605
ExAC:
1:156128220 T / C
gnomAD v2:
1-156128220-T-C
gnomAD v3:
1-156158429-T-C
gnomAD v4:
1-156158429-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156158429T>C , CM000663.2:g.156158429T>C | GRCh38 |
| NC_000001.10:g.156128220T>C , CM000663.1:g.156128220T>C | GRCh37 |
| NC_000001.9:g.154394844T>C | NCBI36 |
| NG_027683.1:g.13486T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368285.8:c.405T>C MANE Select | ENSP00000357268.3:p.Asn135= | |
| ENST00000355014.6:c.405T>C | ENSP00000347117.2:p.Asn135= | |
| ENST00000368282.1:c.405T>C | ENSP00000357265.1:p.Asn135= | |
| ENST00000368284.5:c.67-290T>C | ENSP00000357267.1:n.67-290T>C | |
| ENST00000368285.7:c.405T>C | ENSP00000357268.3:p.Asn135= | |
| ENST00000368286.6:c.291T>C | ENSP00000357269.3:p.Asn97= | |
| ENST00000414683.5:c.108T>C | ENSP00000399230.1:p.Asn36= | |
| ENST00000435124.5:c.405T>C | ENSP00000401391.1:p.Asn135= | |
| ENST00000438830.5:c.364-290T>C | ENSP00000392865.1:n.364-290T>C | |
| ENST00000470306.5:n.1803T>C | ||
| ENST00000487358.5:n.255T>C | ||
| NM_001193300.1:c.405T>C | NP_001180229.1:p.Asn135= | |
| NM_001193301.1:c.405T>C | NP_001180230.1:p.Asn135= | |
| NM_001193302.1:c.67-290T>C | NP_001180231.1:n.67-290T>C | |
| NM_022367.3:c.405T>C | NP_071762.2:p.Asn135= | |
| XM_011509871.1:c.291T>C | XP_011508173.1:p.Asn97= | |
| XM_011509872.1:c.405T>C | XP_011508174.1:p.Asn135= | |
| XM_011509873.1:c.405T>C | XP_011508175.1:p.Asn135= | |
| XM_011509874.1:c.108T>C | XP_011508176.1:p.Asn36= | |
| XM_011509875.1:c.108T>C | XP_011508177.1:p.Asn36= | |
| XM_011509876.1:c.108T>C | XP_011508178.1:p.Asn36= | |
| XM_011509877.1:c.108T>C | XP_011508179.1:p.Asn36= | |
| XM_011509878.1:c.108T>C | XP_011508180.1:p.Asn36= | |
| XM_011509879.1:c.-120T>C | XP_011508181.1:n.-120T>C | |
| XM_011509871.3:c.291T>C | XP_011508173.1:p.Asn97= | |
| XM_011509872.2:c.405T>C | XP_011508174.1:p.Asn135= | |
| XM_011509873.2:c.405T>C | XP_011508175.1:p.Asn135= | |
| XM_011509874.2:c.108T>C | XP_011508176.1:p.Asn36= | |
| XM_011509875.3:c.108T>C | XP_011508177.1:p.Asn36= | |
| XM_011509876.2:c.108T>C | XP_011508178.1:p.Asn36= | |
| XM_011509878.2:c.108T>C | XP_011508180.1:p.Asn36= | |
| XM_011509879.2:c.-120T>C | XP_011508181.1:n.-120T>C | |
| XM_017002056.1:c.405T>C | XP_016857545.1:p.Asn135= | |
| XM_017002057.1:c.-120T>C | XP_016857546.1:n.-120T>C | |
| NM_022367.4:c.405T>C MANE Select | NP_071762.2:p.Asn135= | |
| NM_001193300.2:c.405T>C | NP_001180229.1:p.Asn135= | |
| NM_001370567.1:c.405T>C | NP_001357496.1:p.Asn135= | |
| NM_001370568.1:c.108T>C | NP_001357497.1:p.Asn36= | |
| NM_001370569.1:c.-120T>C | NP_001357498.1:n.-120T>C | |
| NM_001370571.1:c.-120T>C | NP_001357500.1:n.-120T>C | |
| NM_001193301.2:c.405T>C | NP_001180230.1:p.Asn135= | |
| NM_001193302.2:c.67-290T>C | NP_001180231.1:n.67-290T>C |