Linked Data
ClinVar Variation Id:
1256021
ClinVar RCV Id:
RCV001661781
dbSNP Id:
rs1373284153
gnomAD v4:
3-138946170-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138946170C>G , CM000665.2:g.138946170C>G | GRCh38 |
| NC_000003.11:g.138665012C>G , CM000665.1:g.138665012C>G | GRCh37 |
| NC_000003.10:g.140147702C>G | NCBI36 |
| NG_012454.1:g.5971G>C | |
| NG_029796.1:g.3937C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.553G>C MANE Select | ENSP00000497217.1:p.Gly185Arg | |
| ENST00000330315.3:c.553G>C | ENSP00000333188.3:p.Gly185Arg | |
| NM_023067.3:c.553G>C | NP_075555.1:p.Gly185Arg | |
| NM_023067.4:c.553G>C MANE Select | NP_075555.1:p.Gly185Arg |