Linked Data
ClinVar Variation Id:
359595
ClinVar RCV Id:
RCV000318023
dbSNP Id:
rs886062170
gnomAD v4:
7-21545101-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21545101A>G , CM000669.2:g.21545101A>G | GRCh38 |
| NC_000007.13:g.21584719A>G , CM000669.1:g.21584719A>G | GRCh37 |
| NC_000007.12:g.21551244A>G | NCBI36 |
| NG_012886.2:g.6887A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.447A>G MANE Select | ENSP00000475939.1:p.Gly149= | |
| ENST00000328843.10:c.447A>G | ENSP00000330671.7:p.Gly149= | |
| ENST00000409508.7:c.447A>G | ENSP00000475939.1:p.Gly149= | |
| ENST00000607050.1:n.437A>G | ||
| ENST00000620169.4:c.447A>G | ENSP00000481693.1:p.Gly149= | |
| NM_001277115.1:c.447A>G | NP_001264044.1:p.Gly149= | |
| NM_001277115.2:c.447A>G MANE Select | NP_001264044.1:p.Gly149= |