Linked Data
ClinVar Variation Id:
411708
dbSNP Id:
rs769250018
gnomAD v2:
5-156074530-C-T
gnomAD v4:
5-156647520-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.156647520C>T , CM000667.2:g.156647520C>T | GRCh38 |
| NC_000005.9:g.156074530C>T , CM000667.1:g.156074530C>T | GRCh37 |
| NC_000005.8:g.156007108C>T | NCBI36 |
| NG_008693.2:g.782177C>T , LRG_205:g.782177C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000337851.9:c.559C>T MANE Select | ENSP00000338343.4:p.Pro187Ser | |
| ENST00000337851.8:c.559C>T | ENSP00000338343.4:p.Pro187Ser | |
| ENST00000435422.7:c.556C>T | ENSP00000403003.2:p.Pro186Ser | |
| ENST00000517913.5:c.559C>T | ENSP00000429378.1:p.Pro187Ser | |
| NM_000337.5:c.559C>T , LRG_205t1:c.559C>T | NP_000328.2:p.Pro187Ser | |
| NM_001128209.1:c.556C>T | NP_001121681.1:p.Pro186Ser | |
| NM_172244.2:c.559C>T | NP_758447.1:p.Pro187Ser | |
| XM_005265966.3:c.559C>T | XP_005266023.1:p.Pro187Ser | |
| XM_005265967.1:c.502+52469C>T | XP_005266024.1:n.502+52469C>T | |
| XM_006714911.2:c.559C>T | XP_006714974.1:p.Pro187Ser | |
| XM_011534621.1:c.556C>T | XP_011532923.1:p.Pro186Ser | |
| XM_005265966.5:c.559C>T | XP_005266023.1:p.Pro187Ser | |
| XM_005265967.2:c.502+52469C>T | XP_005266024.1:n.502+52469C>T | |
| XM_011534621.2:c.556C>T | XP_011532923.1:p.Pro186Ser | |
| XM_017009723.2:c.559C>T | XP_016865212.1:p.Pro187Ser | |
| XM_017009724.1:c.559C>T | XP_016865213.1:p.Pro187Ser | |
| NM_001128209.2:c.556C>T | NP_001121681.1:p.Pro186Ser | |
| NM_172244.3:c.559C>T | NP_758447.1:p.Pro187Ser | |
| NM_000337.6:c.559C>T MANE Select | NP_000328.2:p.Pro187Ser |