Linked Data
ClinVar Variation Id:
2727350
ClinVar RCV Id:
RCV003526965
dbSNP Id:
rs868508482
gnomAD v2:
5-127640705-T-A
gnomAD v4:
5-128305013-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128305013T>A , CM000667.2:g.128305013T>A | GRCh38 |
| NC_000005.9:g.127640705T>A , CM000667.1:g.127640705T>A | GRCh37 |
| NC_000005.8:g.127668604T>A | NCBI36 |
| NG_008750.1:g.238031A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.2528A>T | ||
| ENST00000703785.1:n.2447A>T | ||
| ENST00000262464.9:c.5744A>T MANE Select | ENSP00000262464.4:p.Tyr1915Phe | |
| ENST00000262464.8:c.5744A>T | ENSP00000262464.4:p.Tyr1915Phe | |
| ENST00000508053.5:c.5744A>T | ENSP00000424571.1:p.Tyr1915Phe | |
| ENST00000619499.4:c.5741A>T | ENSP00000482132.1:p.Tyr1914Phe | |
| NM_001999.3:c.5744A>T | NP_001990.2:p.Tyr1915Phe | |
| XM_017009228.2:c.5591A>T | XP_016864717.1:p.Tyr1864Phe | |
| NM_001999.4:c.5744A>T MANE Select | NP_001990.2:p.Tyr1915Phe |