Linked Data
ClinVar Variation Id:
916074
ClinVar RCV Id:
RCV001171575
dbSNP Id:
rs1028553365
gnomAD v4:
16-1985969-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985969G>T , CM000678.2:g.1985969G>T | GRCh38 |
| NC_000016.9:g.2035970G>T , CM000678.1:g.2035970G>T | GRCh37 |
| NC_000016.8:g.1975971G>T | NCBI36 |
| NG_016288.1:g.6821G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.334G>T | ENSP00000455885.1:p.Asp112Tyr | |
| ENST00000248114.7:c.559G>T MANE Select | ENSP00000248114.6:p.Asp187Tyr | |
| ENST00000248114.6:c.559G>T | ENSP00000248114.6:p.Asp187Tyr | |
| ENST00000565658.1:n.716G>T | ||
| ENST00000567719.1:c.334G>T | ENSP00000455885.1:p.Asp112Tyr | |
| ENST00000569451.1:c.*32G>T | ENSP00000456432.1:n.*32G>T | |
| NM_005262.2:c.559G>T | NP_005253.3:p.Asp187Tyr | |
| NM_005262.3:c.559G>T MANE Select | NP_005253.3:p.Asp187Tyr |