Linked Data
ClinVar Variation Id:
743061
ClinVar RCV Id:
RCV000919383
dbSNP Id:
rs1597592156
gnomAD v4:
17-17219178-G-A
MyVariant Identifiers:
chr17:g.17122492G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.17219178G>A , CM000679.2:g.17219178G>A | GRCh38 |
| NC_000017.10:g.17122492G>A , CM000679.1:g.17122492G>A | GRCh37 |
| NC_000017.9:g.17063217G>A | NCBI36 |
| NG_008001.2:g.23011C>T , LRG_325:g.23011C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285071.9:c.903C>T MANE Select | ENSP00000285071.4:p.Asn301= | |
| ENST00000285071.8:c.903C>T | ENSP00000285071.4:p.Asn301= | |
| ENST00000427497.3:c.149-124C>T | ENSP00000394249.3:n.149-124C>T | |
| NM_144997.5:c.903C>T , LRG_325t1:c.903C>T | NP_659434.2:p.Asn301= | |
| XM_011523714.1:c.957C>T | XP_011522016.1:p.Asn319= | |
| XM_011523715.1:c.957C>T | XP_011522017.1:p.Asn319= | |
| XM_011523716.1:c.957C>T | XP_011522018.1:p.Asn319= | |
| XM_011523717.1:c.957C>T | XP_011522019.1:p.Asn319= | |
| XM_011523718.1:c.957C>T | XP_011522020.1:p.Asn319= | |
| XM_011523719.1:c.957C>T | XP_011522021.1:p.Asn319= | |
| XM_011523720.1:c.681C>T | XP_011522022.1:p.Asn227= | |
| XM_011523721.1:c.957C>T | XP_011522023.1:p.Asn319= | |
| XR_934007.1:n.2297C>T | ||
| NM_001353229.1:c.957C>T | NP_001340158.1:p.Asn319= | |
| NM_001353230.1:c.903C>T | NP_001340159.1:p.Asn301= | |
| NM_001353231.1:c.903C>T | NP_001340160.1:p.Asn301= | |
| NM_144997.6:c.903C>T | NP_659434.2:p.Asn301= | |
| XM_011523714.3:c.957C>T | XP_011522016.1:p.Asn319= | |
| XM_011523718.3:c.957C>T | XP_011522020.1:p.Asn319= | |
| XM_011523719.3:c.957C>T | XP_011522021.1:p.Asn319= | |
| XM_011523721.3:c.957C>T | XP_011522023.1:p.Asn319= | |
| XM_017024305.2:c.957C>T | XP_016879794.1:p.Asn319= | |
| XM_017024308.1:c.903C>T | XP_016879797.1:p.Asn301= | |
| XM_017024309.2:c.681C>T | XP_016879798.1:p.Asn227= | |
| XM_024450635.1:c.957C>T | XP_024306403.1:p.Asn319= | |
| XR_001752445.2:n.1461C>T | ||
| NM_144997.7:c.903C>T MANE Select | NP_659434.2:p.Asn301= | |
| NM_001353229.2:c.957C>T | NP_001340158.1:p.Asn319= | |
| NM_001353230.2:c.903C>T | NP_001340159.1:p.Asn301= | |
| NM_001353231.2:c.903C>T | NP_001340160.1:p.Asn301= |