This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.03253595 (AFR)
Genomes Max Group AF
0.0324849 (AFR)
Exomes Max Group AF
0.03160005 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.165901737G>A , CM000664.2:g.165901737G>A | GRCh38 |
| NC_000002.11:g.166758247G>A , CM000664.1:g.166758247G>A | GRCh37 |
| NC_000002.10:g.166466493G>A | NCBI36 |
| NG_030345.1:g.57102C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243344.8:c.2742C>T MANE Select | ENSP00000243344.7:p.Cys914= | |
| ENST00000652557.1:c.2742C>T | ENSP00000498617.1:p.Cys914= | |
| ENST00000679356.1:c.2742C>T | ENSP00000506245.1:p.Cys914= | |
| ENST00000679676.1:c.2631C>T | ENSP00000505492.1:p.Cys877= | |
| ENST00000679799.1:c.2742C>T | ENSP00000505208.1:p.Cys914= | |
| ENST00000679840.1:c.2742C>T | ENSP00000505248.1:p.Cys914= | |
| ENST00000679931.1:c.*1784C>T | ENSP00000505632.1:n.*1784C>T | |
| ENST00000679967.1:c.2742C>T | ENSP00000506607.1:p.Cys914= | |
| ENST00000680327.1:c.*1784C>T | ENSP00000506639.1:n.*1784C>T | |
| ENST00000680448.1:c.2742C>T | ENSP00000505921.1:p.Cys914= | |
| ENST00000680657.1:n.2853C>T | ||
| ENST00000680690.1:c.*1994C>T | ENSP00000506121.1:n.*1994C>T | |
| ENST00000680888.1:c.2742C>T | ENSP00000506276.1:p.Cys914= | |
| ENST00000680925.1:n.741C>T | ||
| ENST00000680947.1:c.*2014C>T | ENSP00000506496.1:n.*2014C>T | |
| ENST00000681024.1:c.2742C>T | ENSP00000506449.1:p.Cys914= | |
| ENST00000681083.1:c.*2476C>T | ENSP00000506095.1:n.*2476C>T | |
| ENST00000681167.1:n.2616C>T | ||
| ENST00000681483.1:c.2742C>T | ENSP00000505499.1:p.Cys914= | |
| ENST00000681502.1:c.*2166C>T | ENSP00000505644.1:n.*2166C>T | |
| ENST00000681606.1:c.2742C>T | ENSP00000505354.1:p.Cys914= | |
| ENST00000681819.1:c.2742C>T | ENSP00000505673.1:p.Cys914= | |
| ENST00000681952.1:c.2742C>T | ENSP00000506400.1:p.Cys914= | |
| ENST00000243344.7:c.2742C>T | ENSP00000243344.7:p.Cys914= | |
| ENST00000484129.1:n.217C>T | ||
| NM_024753.4:c.2742C>T | NP_079029.3:p.Cys914= | |
| XM_006712761.1:c.2742C>T | XP_006712824.1:p.Cys914= | |
| XM_011511870.1:c.2175C>T | XP_011510172.1:p.Cys725= | |
| XM_011511871.1:c.1992C>T | XP_011510173.1:p.Cys664= | |
| XM_011511872.1:c.2742C>T | XP_011510174.1:p.Cys914= | |
| XM_011511871.3:c.1992C>T | XP_011510173.1:p.Cys664= | |
| XM_011511872.2:c.2742C>T | XP_011510174.1:p.Cys914= | |
| XM_017004967.1:c.2742C>T | XP_016860456.1:p.Cys914= | |
| XM_017004968.2:c.2088C>T | XP_016860457.1:p.Cys696= | |
| XM_017004969.1:c.1743C>T | XP_016860458.1:p.Cys581= | |
| NM_024753.5:c.2742C>T MANE Select | NP_079029.3:p.Cys914= |