Linked Data
ClinVar Variation Id:
6420
ClinVar RCV Id:
RCV002226443
dbSNP Id:
rs121908888
gnomAD v2:
5-131719973-A-G
gnomAD v3:
5-132384281-A-G
gnomAD v4:
5-132384281-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132384281A>G , CM000667.2:g.132384281A>G | GRCh38 |
| NC_000005.9:g.131719973A>G , CM000667.1:g.131719973A>G | GRCh37 |
| NC_000005.8:g.131747872A>G | NCBI36 |
| NG_008982.1:g.19573A>G | |
| NG_008982.2:g.19578A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000415928.6:c.632A>G | ENSP00000388838.2:p.Tyr211Cys | |
| ENST00000435065.7:c.704A>G | ENSP00000402760.2:p.Tyr235Cys | |
| ENST00000448810.6:c.632A>G | ENSP00000401860.2:p.Tyr211Cys | |
| ENST00000686757.1:c.632A>G | ENSP00000510721.1:p.Tyr211Cys | |
| ENST00000687740.1:n.766A>G | ||
| ENST00000688151.1:n.1811A>G | ||
| ENST00000689271.1:c.632A>G | ENSP00000510797.1:p.Tyr211Cys | |
| ENST00000690900.1:c.632A>G | ENSP00000510703.1:p.Tyr211Cys | |
| ENST00000692355.1:c.184A>G | ||
| ENST00000692413.1:c.632A>G | ENSP00000509374.1:p.Tyr211Cys | |
| ENST00000692825.1:c.700A>G | ENSP00000509447.1:n.700A>G | |
| ENST00000693308.1:c.632A>G | ENSP00000509770.1:p.Tyr211Cys | |
| ENST00000693763.1:n.766A>G | ||
| ENST00000245407.8:c.632A>G MANE Select | ENSP00000245407.3:p.Tyr211Cys | |
| ENST00000245407.7:c.632A>G | ENSP00000245407.3:p.Tyr211Cys | |
| ENST00000415928.5:c.401A>G | ENSP00000388838.1:p.Tyr134Cys | |
| ENST00000435065.6:c.704A>G | ENSP00000402760.2:p.Tyr235Cys | |
| ENST00000437841.6:c.394-1047A>G | ENSP00000400553.1:n.394-1047A>G | |
| ENST00000461013.5:n.8054A>G | ||
| NM_001308122.1:c.704A>G | NP_001295051.1:p.Tyr235Cys | |
| NM_003060.3:c.632A>G | NP_003051.1:p.Tyr211Cys | |
| XM_011543590.1:c.1A>G | XP_011541892.1:p.Met1Val | |
| XR_427718.1:n.973A>G | ||
| XR_948290.1:n.973A>G | ||
| XR_948291.1:n.973A>G | ||
| XM_011543590.2:c.1A>G | XP_011541892.1:p.Met1Val | |
| XM_017009778.2:c.104A>G | XP_016865267.1:p.Tyr35Cys | |
| XR_001742215.1:n.973A>G | ||
| XR_001742216.1:n.973A>G | ||
| XR_427718.2:n.973A>G | ||
| XR_948290.2:n.973A>G | ||
| XR_948291.2:n.973A>G | ||
| NM_003060.4:c.632A>G MANE Select | NP_003051.1:p.Tyr211Cys | |
| NM_001308122.2:c.704A>G | NP_001295051.1:p.Tyr235Cys |