Linked Data
dbSNP Id:
rs1664784115
gnomAD v3:
2-26467401-G-A
gnomAD v4:
2-26467401-G-A
MyVariant Identifiers:
chr2:g.26690269G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26467401G>A , CM000664.2:g.26467401G>A | GRCh38 |
| NC_000002.11:g.26690269G>A , CM000664.1:g.26690269G>A | GRCh37 |
| NC_000002.10:g.26543773G>A | NCBI36 |
| NG_009937.1:g.96298C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272371.7:c.4191C>T MANE Select | ENSP00000272371.2:p.Ala1397= | |
| ENST00000339598.8:c.1890C>T MANE Plus Clinical | ENSP00000344521.3:p.Ala630= | |
| ENST00000402415.8:c.1950C>T | ENSP00000383906.4:p.Ala650= | |
| ENST00000272371.6:c.4191C>T | ENSP00000272371.2:p.Ala1397= | |
| ENST00000338581.10:c.1890C>T | ENSP00000345137.6:p.Ala630= | |
| ENST00000339598.7:c.1890C>T | ENSP00000344521.3:p.Ala630= | |
| ENST00000402415.7:c.2121C>T | ENSP00000383906.3:p.Ala707= | |
| ENST00000403946.7:c.4191C>T | ENSP00000385255.3:p.Ala1397= | |
| NM_001287489.1:c.4191C>T | NP_001274418.1:p.Ala1397= | |
| NM_004802.3:c.1890C>T | NP_004793.2:p.Ala630= | |
| NM_194248.2:c.4191C>T | NP_919224.1:p.Ala1397= | |
| NM_194322.2:c.2121C>T | NP_919303.1:p.Ala707= | |
| NM_194323.2:c.1890C>T | NP_919304.1:p.Ala630= | |
| XM_005264644.2:c.4176C>T | XP_005264701.1:p.Ala1392= | |
| XM_011533185.1:c.4236C>T | XP_011531487.1:p.Ala1412= | |
| XM_017005338.1:c.4131C>T | XP_016860827.1:p.Ala1377= | |
| NM_001287489.2:c.4191C>T | NP_001274418.1:p.Ala1397= | |
| NM_004802.4:c.1890C>T | NP_004793.2:p.Ala630= | |
| NM_194248.3:c.4191C>T MANE Select | NP_919224.1:p.Ala1397= | |
| NM_194322.3:c.2121C>T | NP_919303.1:p.Ala707= | |
| NM_194323.3:c.1890C>T MANE Plus Clinical | NP_919304.1:p.Ala630= |