Linked Data
dbSNP Id:
rs933757221
gnomAD v4:
11-822197-C-T
MyVariant Identifiers:
chr11:g.822197C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.822197C>T , CM000673.2:g.822197C>T | GRCh38 |
| NC_000011.9:g.822197C>T , CM000673.1:g.822197C>T | GRCh37 |
| NC_000011.8:g.812197C>T | NCBI36 |
| NG_023394.1:g.8297C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336615.9:c.486+174C>T MANE Select | ENSP00000337701.4:n.486+174C>T | |
| ENST00000336615.8:c.486+174C>T | ENSP00000337701.4:n.486+174C>T | |
| ENST00000525250.5:n.1092+174C>T | ||
| ENST00000531923.1:n.182C>T | ||
| ENST00000534561.1:n.327C>T | ||
| ENST00000617551.1:c.-765+174C>T | ENSP00000481602.1:n.-765+174C>T | |
| NM_020376.3:c.486+174C>T | NP_065109.1:n.486+174C>T | |
| XM_006718265.2:c.486+174C>T | XP_006718328.1:n.486+174C>T | |
| XM_006718266.2:c.486+174C>T | XP_006718329.1:n.486+174C>T | |
| XM_006718265.3:c.486+174C>T | XP_006718328.1:n.486+174C>T | |
| XM_006718266.3:c.486+174C>T | XP_006718329.1:n.486+174C>T | |
| XM_017018028.1:c.486+174C>T | XP_016873517.1:n.486+174C>T | |
| XM_024448618.1:c.486+174C>T | XP_024304386.1:n.486+174C>T | |
| NM_020376.4:c.486+174C>T MANE Select | NP_065109.1:n.486+174C>T |