Linked Data
ClinVar Variation Id:
528907
ClinVar RCV Id:
RCV000634200
dbSNP Id:
rs1553508246
gnomAD v4:
2-165898769-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.165898769T>C , CM000664.2:g.165898769T>C | GRCh38 |
| NC_000002.11:g.166755279T>C , CM000664.1:g.166755279T>C | GRCh37 |
| NC_000002.10:g.166463525T>C | NCBI36 |
| NG_030345.1:g.60070A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243344.8:c.2869-2A>G MANE Select | ENSP00000243344.7:n.2869-2A>G | |
| ENST00000652557.1:c.2869-2A>G | ENSP00000498617.1:n.2869-2A>G | |
| ENST00000679356.1:c.2869-2A>G | ENSP00000506245.1:n.2869-2A>G | |
| ENST00000679676.1:c.2758-2A>G | ENSP00000505492.1:n.2758-2A>G | |
| ENST00000679799.1:c.2869-2A>G | ENSP00000505208.1:n.2869-2A>G | |
| ENST00000679840.1:c.2869-2A>G | ENSP00000505248.1:n.2869-2A>G | |
| ENST00000679931.1:c.*1911-2A>G | ENSP00000505632.1:n.*1911-2A>G | |
| ENST00000679967.1:c.2869-2A>G | ENSP00000506607.1:n.2869-2A>G | |
| ENST00000680327.1:c.*1911-2A>G | ENSP00000506639.1:n.*1911-2A>G | |
| ENST00000680448.1:c.2869-2A>G | ENSP00000505921.1:n.2869-2A>G | |
| ENST00000680657.1:n.2980-2A>G | ||
| ENST00000680690.1:c.*2121-2A>G | ENSP00000506121.1:n.*2121-2A>G | |
| ENST00000680888.1:c.2869-2A>G | ENSP00000506276.1:n.2869-2A>G | |
| ENST00000680925.1:n.899-2A>G | ||
| ENST00000680947.1:c.*2141-2A>G | ENSP00000506496.1:n.*2141-2A>G | |
| ENST00000681024.1:c.2869-2A>G | ENSP00000506449.1:n.2869-2A>G | |
| ENST00000681083.1:c.*2603-2A>G | ENSP00000506095.1:n.*2603-2A>G | |
| ENST00000681167.1:n.2743-2A>G | ||
| ENST00000681483.1:c.2869-2A>G | ENSP00000505499.1:n.2869-2A>G | |
| ENST00000681502.1:c.*2293-2A>G | ENSP00000505644.1:n.*2293-2A>G | |
| ENST00000681606.1:c.2869-2A>G | ENSP00000505354.1:n.2869-2A>G | |
| ENST00000681819.1:c.2869-2A>G | ENSP00000505673.1:n.2869-2A>G | |
| ENST00000681952.1:c.2869-2A>G | ENSP00000506400.1:n.2869-2A>G | |
| ENST00000243344.7:c.2869-2A>G | ENSP00000243344.7:n.2869-2A>G | |
| ENST00000484129.1:n.344-2A>G | ||
| NM_024753.4:c.2869-2A>G | NP_079029.3:n.2869-2A>G | |
| XM_006712761.1:c.2869-2A>G | XP_006712824.1:n.2869-2A>G | |
| XM_011511870.1:c.2302-2A>G | XP_011510172.1:n.2302-2A>G | |
| XM_011511871.1:c.2119-2A>G | XP_011510173.1:n.2119-2A>G | |
| XM_011511872.1:c.*71-2A>G | XP_011510174.1:n.*71-2A>G | |
| XM_011511871.3:c.2119-2A>G | XP_011510173.1:n.2119-2A>G | |
| XM_011511872.2:c.*71-2A>G | XP_011510174.1:n.*71-2A>G | |
| XM_017004967.1:c.2869-2A>G | XP_016860456.1:n.2869-2A>G | |
| XM_017004968.2:c.2215-2A>G | XP_016860457.1:n.2215-2A>G | |
| XM_017004969.1:c.1870-2A>G | XP_016860458.1:n.1870-2A>G | |
| NM_024753.5:c.2869-2A>G MANE Select | NP_079029.3:n.2869-2A>G |