ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55151898T>C , CM000681.2:g.55151898T>C | GRCh38 |
| NC_000019.9:g.55663266T>C , CM000681.1:g.55663266T>C | GRCh37 |
| NC_000019.8:g.60355078T>C | NCBI36 |
| NG_007866.2:g.10835A>G , LRG_432:g.10835A>G | |
| NG_011829.2:g.2341A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.569A>G MANE Select | ENSP00000341838.5:p.Asp190Gly | |
| ENST00000665070.1:c.602A>G | ENSP00000499482.1:p.Asp201Gly | |
| ENST00000344887.9:c.569A>G | ENSP00000341838.5:p.Asp190Gly | |
| ENST00000585806.5:n.568A>G | ||
| ENST00000588882.1:c.494A>G | ENSP00000466729.1:p.Asp165Gly | |
| ENST00000589864.1:n.397A>G | ||
| NM_000363.4:c.569A>G , LRG_432t1:c.569A>G | NP_000354.4:p.Asp190Gly | |
| NM_000363.5:c.569A>G MANE Select | NP_000354.4:p.Asp190Gly |