Linked Data
dbSNP Id:
rs2089573717
gnomAD v3:
20-25078898-G-A
gnomAD v4:
20-25078898-G-A
MyVariant Identifiers:
chr20:g.25059534G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.25078898G>A , CM000682.2:g.25078898G>A | GRCh38 |
| NC_000020.10:g.25059534G>A , CM000682.1:g.25059534G>A | GRCh37 |
| NC_000020.9:g.25007534G>A | NCBI36 |
| NG_008101.1:g.8234C>T | |
| NG_008101.2:g.8234C>T | |
| NG_008101.3:g.8284C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376709.9:c.558C>T MANE Select | ENSP00000365899.3:p.Ala186= | |
| ENST00000376707.4:c.558C>T | ENSP00000365897.3:p.Ala186= | |
| ENST00000376709.8:c.558C>T | ENSP00000365899.3:p.Ala186= | |
| ENST00000409285.6:c.558C>T | ENSP00000386612.2:p.Ala186= | |
| ENST00000409958.6:c.558C>T | ENSP00000387069.2:p.Ala186= | |
| ENST00000429762.7:c.558C>T | ENSP00000401690.3:p.Ala186= | |
| ENST00000444511.6:c.558C>T | ENSP00000387720.2:p.Ala186= | |
| NM_001256271.1:c.558C>T | NP_001243200.1:p.Ala186= | |
| NM_001256272.1:c.558C>T | NP_001243201.1:p.Ala186= | |
| NM_014588.5:c.558C>T | NP_055403.2:p.Ala186= | |
| NM_199425.2:c.558C>T | NP_955457.1:p.Ala186= | |
| NR_045948.1:n.841C>T | ||
| NR_045951.1:n.841C>T | ||
| XM_017027837.1:c.558C>T | XP_016883326.1:p.Ala186= | |
| XM_017027838.1:c.558C>T | XP_016883327.1:p.Ala186= | |
| NM_014588.6:c.558C>T MANE Select | NP_055403.2:p.Ala186= | |
| NR_165181.1:n.316C>T | ||
| NM_001256271.2:c.558C>T | NP_001243200.1:p.Ala186= | |
| NM_001256272.2:c.558C>T | NP_001243201.1:p.Ala186= | |
| NM_199425.3:c.558C>T | NP_955457.1:p.Ala186= | |
| NR_045948.2:n.603C>T | ||
| NR_045951.2:n.603C>T | ||
| NR_165181.2:n.198C>T |