Linked Data
dbSNP Id:
rs770730662
ExAC:
20:62038661 G / T
gnomAD v2:
20-62038661-G-T
gnomAD v4:
20-63407308-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63407308G>T , CM000682.2:g.63407308G>T | GRCh38 |
| NC_000020.10:g.62038661G>T , CM000682.1:g.62038661G>T | GRCh37 |
| NC_000020.9:g.61509105G>T | NCBI36 |
| NG_009004.1:g.70333C>A | |
| NG_009004.2:g.70333C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706989.1:c.2009C>A | ENSP00000516702.1:p.Pro670Gln | |
| ENST00000359125.7:c.1955C>A MANE Select | ENSP00000352035.2:p.Pro652Gln | |
| ENST00000637193.1:c.1352C>A | ENSP00000490734.1:p.Pro451Gln | |
| ENST00000344462.8:c.1862C>A | ENSP00000339611.4:p.Pro621Gln | |
| ENST00000357249.6:c.1523C>A | ENSP00000349789.3:p.Pro508Gln | |
| ENST00000359125.6:c.1955C>A | ENSP00000352035.2:p.Pro652Gln | |
| ENST00000360480.7:c.1871C>A | ENSP00000353668.3:p.Pro624Gln | |
| ENST00000370224.5:c.1979C>A | ENSP00000359244.2:p.Pro660Gln | |
| ENST00000625514.2:c.1943C>A | ENSP00000486040.1:p.Pro648Gln | |
| ENST00000626839.2:c.1901C>A | ENSP00000486706.1:p.Pro634Gln | |
| ENST00000629241.2:c.1871C>A | ENSP00000487142.1:p.Pro624Gln | |
| ENST00000629676.2:c.1679+6142C>A | ENSP00000486194.1:n.1679+6142C>A | |
| NM_004518.4:c.1871C>A | NP_004509.2:p.Pro624Gln | |
| NM_172106.1:c.1901C>A | NP_742104.1:p.Pro634Gln | |
| NM_172107.2:c.1955C>A | NP_742105.1:p.Pro652Gln | |
| NM_172108.3:c.1862C>A | NP_742106.1:p.Pro621Gln | |
| XM_006723787.1:c.1997C>A | XP_006723850.1:p.Pro666Gln | |
| XM_011528807.1:c.2063C>A | XP_011527109.1:p.Pro688Gln | |
| XM_011528808.1:c.2060C>A | XP_011527110.1:p.Pro687Gln | |
| XM_011528809.1:c.2033C>A | XP_011527111.1:p.Pro678Gln | |
| XM_011528810.1:c.2009C>A | XP_011527112.1:p.Pro670Gln | |
| XM_011528811.1:c.1979C>A | XP_011527113.1:p.Pro660Gln | |
| XM_011528812.1:c.1952C>A | XP_011527114.1:p.Pro651Gln | |
| XM_011528813.1:c.1937C>A | XP_011527115.1:p.Pro646Gln | |
| XM_011528814.1:c.1544C>A | XP_011527116.1:p.Pro515Gln | |
| NM_004518.5:c.1871C>A | NP_004509.2:p.Pro624Gln | |
| NM_172106.2:c.1901C>A | NP_742104.1:p.Pro634Gln | |
| NM_172107.3:c.1955C>A | NP_742105.1:p.Pro652Gln | |
| NM_172108.4:c.1862C>A | NP_742106.1:p.Pro621Gln | |
| XM_011528810.2:c.2009C>A | XP_011527112.1:p.Pro670Gln | |
| XM_011528811.2:c.1979C>A | XP_011527113.1:p.Pro660Gln | |
| XM_017027841.2:c.2006C>A | XP_016883330.1:p.Pro669Gln | |
| XM_017027842.2:c.1943C>A | XP_016883331.1:p.Pro648Gln | |
| XM_017027843.1:c.1940C>A | XP_016883332.1:p.Pro647Gln | |
| XM_017027844.2:c.1898C>A | XP_016883333.1:p.Pro633Gln | |
| XM_017027845.1:c.971C>A | XP_016883334.1:p.Pro324Gln | |
| NM_004518.6:c.1871C>A | NP_004509.2:p.Pro624Gln | |
| NM_172106.3:c.1901C>A | NP_742104.1:p.Pro634Gln | |
| NM_172107.4:c.1955C>A MANE Select | NP_742105.1:p.Pro652Gln | |
| NM_172108.5:c.1862C>A | NP_742106.1:p.Pro621Gln | |
| NM_001382235.1:c.2009C>A | NP_001369164.1:p.Pro670Gln |