Linked Data
ClinVar Variation Id:
2955458
ClinVar RCV Id:
RCV003818633
dbSNP Id:
rs780234165
gnomAD v4:
2-26475983-G-C
MyVariant Identifiers:
chr2:g.26698851G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26475983G>C , CM000664.2:g.26475983G>C | GRCh38 |
| NC_000002.11:g.26698851G>C , CM000664.1:g.26698851G>C | GRCh37 |
| NC_000002.10:g.26552355G>C | NCBI36 |
| NG_009937.1:g.87716C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000272371.7:c.2922C>G MANE Select | ENSP00000272371.2:p.Ala974= | |
| ENST00000339598.8:c.681C>G MANE Plus Clinical | ENSP00000344521.3:p.Ala227= | |
| ENST00000402415.8:c.681C>G | ENSP00000383906.4:p.Ala227= | |
| ENST00000272371.6:c.2922C>G | ENSP00000272371.2:p.Ala974= | |
| ENST00000338581.10:c.681C>G | ENSP00000345137.6:p.Ala227= | |
| ENST00000339598.7:c.681C>G | ENSP00000344521.3:p.Ala227= | |
| ENST00000402415.7:c.852C>G | ENSP00000383906.3:p.Ala284= | |
| ENST00000403946.7:c.2922C>G | ENSP00000385255.3:p.Ala974= | |
| NM_001287489.1:c.2922C>G | NP_001274418.1:p.Ala974= | |
| NM_004802.3:c.681C>G | NP_004793.2:p.Ala227= | |
| NM_194248.2:c.2922C>G | NP_919224.1:p.Ala974= | |
| NM_194322.2:c.852C>G | NP_919303.1:p.Ala284= | |
| NM_194323.2:c.681C>G | NP_919304.1:p.Ala227= | |
| XM_005264644.2:c.2967C>G | XP_005264701.1:p.Ala989= | |
| XM_011533185.1:c.2967C>G | XP_011531487.1:p.Ala989= | |
| XM_017005338.1:c.2922C>G | XP_016860827.1:p.Ala974= | |
| NM_001287489.2:c.2922C>G | NP_001274418.1:p.Ala974= | |
| NM_004802.4:c.681C>G | NP_004793.2:p.Ala227= | |
| NM_194248.3:c.2922C>G MANE Select | NP_919224.1:p.Ala974= | |
| NM_194322.3:c.852C>G | NP_919303.1:p.Ala284= | |
| NM_194323.3:c.681C>G MANE Plus Clinical | NP_919304.1:p.Ala227= |