Linked Data
ClinVar Variation Id:
1105759
dbSNP Id:
rs1752497453
MyVariant Identifiers:
chr5:g.131721186C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132385494C>G , CM000667.2:g.132385494C>G | GRCh38 |
| NC_000005.9:g.131721186C>G , CM000667.1:g.131721186C>G | GRCh37 |
| NC_000005.8:g.131749085C>G | NCBI36 |
| NG_008982.1:g.20786C>G | |
| NG_008982.2:g.20791C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415928.6:c.665+1180C>G | ENSP00000388838.2:n.665+1180C>G | |
| ENST00000435065.7:c.891C>G | ENSP00000402760.2:p.Leu297= | |
| ENST00000448810.6:c.819C>G | ENSP00000401860.2:p.Leu273= | |
| ENST00000686757.1:c.838C>G | ENSP00000510721.1:p.Leu280Val | |
| ENST00000687740.1:n.1979C>G | ||
| ENST00000688151.1:n.2011C>G | ||
| ENST00000689271.1:c.671+1174C>G | ENSP00000510797.1:n.671+1174C>G | |
| ENST00000690900.1:c.790C>G | ENSP00000510703.1:p.Leu264Val | |
| ENST00000692212.1:n.645C>G | ||
| ENST00000692355.1:c.204+1193C>G | ||
| ENST00000692413.1:c.838C>G | ENSP00000509374.1:p.Leu280Val | |
| ENST00000692825.1:c.887C>G | ENSP00000509447.1:n.887C>G | |
| ENST00000693308.1:c.832C>G | ENSP00000509770.1:p.Leu278Val | |
| ENST00000693763.1:n.1979C>G | ||
| ENST00000245407.8:c.819C>G MANE Select | ENSP00000245407.3:p.Leu273= | |
| ENST00000245407.7:c.819C>G | ENSP00000245407.3:p.Leu273= | |
| ENST00000415928.5:c.588C>G | ENSP00000388838.1:p.Leu196= | |
| ENST00000435065.6:c.891C>G | ENSP00000402760.2:p.Leu297= | |
| ENST00000437841.6:c.*134C>G | ENSP00000400553.1:n.*134C>G | |
| ENST00000448810.5:c.167C>G | ||
| ENST00000461013.5:n.8241C>G | ||
| NM_001308122.1:c.891C>G | NP_001295051.1:p.Leu297= | |
| NM_003060.3:c.819C>G | NP_003051.1:p.Leu273= | |
| XM_011543590.1:c.201C>G | XP_011541892.1:p.Leu67= | |
| XR_427718.1:n.1179C>G | ||
| XR_948290.1:n.1160C>G | ||
| XR_948291.1:n.1173C>G | ||
| XM_011543590.2:c.201C>G | XP_011541892.1:p.Leu67= | |
| XM_017009778.2:c.291C>G | XP_016865267.1:p.Leu97= | |
| XR_001742215.1:n.1160C>G | ||
| XR_001742216.1:n.1179C>G | ||
| XR_427718.2:n.1179C>G | ||
| XR_948290.2:n.1160C>G | ||
| XR_948291.2:n.1173C>G | ||
| NM_003060.4:c.819C>G MANE Select | NP_003051.1:p.Leu273= | |
| NM_001308122.2:c.891C>G | NP_001295051.1:p.Leu297= |