gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00004515 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Exomes Max Group AF
0.00004617 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63408458G>A , CM000682.2:g.63408458G>A | GRCh38 |
| NC_000020.10:g.62039811G>A , CM000682.1:g.62039811G>A | GRCh37 |
| NC_000020.9:g.61510255G>A | NCBI36 |
| NG_009004.1:g.69183C>T | |
| NG_009004.2:g.69183C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706989.1:c.1896C>T | ENSP00000516702.1:p.Pro632= | |
| ENST00000359125.7:c.1842C>T MANE Select | ENSP00000352035.2:p.Pro614= | |
| ENST00000637063.1:n.27C>T | ||
| ENST00000637193.1:c.1239C>T | ENSP00000490734.1:p.Pro413= | |
| ENST00000344462.8:c.1749C>T | ENSP00000339611.4:p.Pro583= | |
| ENST00000357249.6:c.1410C>T | ENSP00000349789.3:p.Pro470= | |
| ENST00000359125.6:c.1842C>T | ENSP00000352035.2:p.Pro614= | |
| ENST00000360480.7:c.1758C>T | ENSP00000353668.3:p.Pro586= | |
| ENST00000370224.5:c.1866C>T | ENSP00000359244.2:p.Pro622= | |
| ENST00000625514.2:c.1830C>T | ENSP00000486040.1:p.Pro610= | |
| ENST00000626839.2:c.1788C>T | ENSP00000486706.1:p.Pro596= | |
| ENST00000629241.2:c.1758C>T | ENSP00000487142.1:p.Pro586= | |
| ENST00000629676.2:c.1679+4992C>T | ENSP00000486194.1:n.1679+4992C>T | |
| NM_004518.4:c.1758C>T | NP_004509.2:p.Pro586= | |
| NM_172106.1:c.1788C>T | NP_742104.1:p.Pro596= | |
| NM_172107.2:c.1842C>T | NP_742105.1:p.Pro614= | |
| NM_172108.3:c.1749C>T | NP_742106.1:p.Pro583= | |
| XM_006723787.1:c.1884C>T | XP_006723850.1:p.Pro628= | |
| XM_011528807.1:c.1950C>T | XP_011527109.1:p.Pro650= | |
| XM_011528808.1:c.1947C>T | XP_011527110.1:p.Pro649= | |
| XM_011528809.1:c.1920C>T | XP_011527111.1:p.Pro640= | |
| XM_011528810.1:c.1896C>T | XP_011527112.1:p.Pro632= | |
| XM_011528811.1:c.1866C>T | XP_011527113.1:p.Pro622= | |
| XM_011528812.1:c.1839C>T | XP_011527114.1:p.Pro613= | |
| XM_011528813.1:c.1824C>T | XP_011527115.1:p.Pro608= | |
| XM_011528814.1:c.1431C>T | XP_011527116.1:p.Pro477= | |
| XM_011528815.1:c.1950C>T | XP_011527117.1:p.Pro650= | |
| NM_004518.5:c.1758C>T | NP_004509.2:p.Pro586= | |
| NM_172106.2:c.1788C>T | NP_742104.1:p.Pro596= | |
| NM_172107.3:c.1842C>T | NP_742105.1:p.Pro614= | |
| NM_172108.4:c.1749C>T | NP_742106.1:p.Pro583= | |
| XM_011528810.2:c.1896C>T | XP_011527112.1:p.Pro632= | |
| XM_011528811.2:c.1866C>T | XP_011527113.1:p.Pro622= | |
| XM_017027841.2:c.1893C>T | XP_016883330.1:p.Pro631= | |
| XM_017027842.2:c.1830C>T | XP_016883331.1:p.Pro610= | |
| XM_017027843.1:c.1827C>T | XP_016883332.1:p.Pro609= | |
| XM_017027844.2:c.1785C>T | XP_016883333.1:p.Pro595= | |
| XM_017027845.1:c.858C>T | XP_016883334.1:p.Pro286= | |
| NM_004518.6:c.1758C>T | NP_004509.2:p.Pro586= | |
| NM_172106.3:c.1788C>T | NP_742104.1:p.Pro596= | |
| NM_172107.4:c.1842C>T MANE Select | NP_742105.1:p.Pro614= | |
| NM_172108.5:c.1749C>T | NP_742106.1:p.Pro583= | |
| NM_001382235.1:c.1896C>T | NP_001369164.1:p.Pro632= |