Linked Data
dbSNP Id:
rs782436372
gnomAD v4:
3-50256213-T-G
MyVariant Identifiers:
chr3:g.50293645T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.50256213T>G , CM000665.2:g.50256213T>G | GRCh38 |
| NC_000003.11:g.50293645T>G , CM000665.1:g.50293645T>G | GRCh37 |
| NC_000003.10:g.50268649T>G | NCBI36 |
| NG_016002.2:g.34526T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313601.11:c.486T>G MANE Select | ENSP00000312999.6:p.Arg162= | |
| ENST00000266027.9:c.330T>G | ENSP00000266027.6:p.Arg110= | |
| ENST00000313601.10:c.486T>G | ENSP00000312999.6:p.Arg162= | |
| ENST00000422163.5:c.438T>G | ENSP00000406871.1:p.Arg146= | |
| ENST00000440628.5:c.330T>G | ENSP00000395736.1:p.Arg110= | |
| ENST00000441156.5:c.*14T>G | ENSP00000394321.1:n.*14T>G | |
| ENST00000446079.5:c.*121T>G | ENSP00000406065.1:n.*121T>G | |
| ENST00000451956.1:c.375T>G | ENSP00000406369.1:p.Arg125= | |
| ENST00000468422.1:n.53T>G | ||
| ENST00000490122.5:n.1313T>G | ||
| ENST00000491100.5:n.2302T>G | ||
| NM_001166425.1:c.375T>G | NP_001159897.1:p.Arg125= | |
| NM_001282617.1:c.330T>G | NP_001269546.1:p.Arg110= | |
| NM_001282618.1:c.243T>G | NP_001269547.1:p.Arg81= | |
| NM_001282619.1:c.438T>G | NP_001269548.1:p.Arg146= | |
| NM_001282620.1:c.438T>G | NP_001269549.1:p.Arg146= | |
| NM_002070.3:c.486T>G | NP_002061.1:p.Arg162= | |
| NM_002070.4:c.486T>G MANE Select | NP_002061.1:p.Arg162= | |
| NM_001166425.2:c.375T>G | NP_001159897.1:p.Arg125= | |
| NM_001282618.2:c.243T>G | NP_001269547.1:p.Arg81= | |
| NM_001282619.2:c.438T>G | NP_001269548.1:p.Arg146= | |
| NM_001282620.2:c.438T>G | NP_001269549.1:p.Arg146= | |
| NM_001282617.2:c.330T>G | NP_001269546.1:p.Arg110= |