Linked Data
dbSNP Id:
rs1935959298
gnomAD v4:
3-138946045-A-C
MyVariant Identifiers:
chr3:g.138664887A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138946045A>C , CM000665.2:g.138946045A>C | GRCh38 |
| NC_000003.11:g.138664887A>C , CM000665.1:g.138664887A>C | GRCh37 |
| NC_000003.10:g.140147577A>C | NCBI36 |
| NG_012454.1:g.6096T>G | |
| NG_029796.1:g.3812A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.678T>G MANE Select | ENSP00000497217.1:p.Ala226= | |
| ENST00000330315.3:c.678T>G | ENSP00000333188.3:p.Ala226= | |
| NM_023067.3:c.678T>G | NP_075555.1:p.Ala226= | |
| NM_023067.4:c.678T>G MANE Select | NP_075555.1:p.Ala226= |