Linked Data
dbSNP Id:
rs995322549
gnomAD v4:
3-165830605-A-T
MyVariant Identifiers:
chr3:g.165548393A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165830605A>T , CM000665.2:g.165830605A>T | GRCh38 |
| NC_000003.11:g.165548393A>T , CM000665.1:g.165548393A>T | GRCh37 |
| NC_000003.10:g.167031087A>T | NCBI36 |
| NG_009031.1:g.11861T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264381.8:c.429T>A MANE Select | ENSP00000264381.3:p.Gly143= | |
| ENST00000264381.7:c.429T>A | ENSP00000264381.3:p.Gly143= | |
| ENST00000479451.5:c.107+6709T>A | ENSP00000418325.1:n.107+6709T>A | |
| ENST00000482958.1:c.429T>A | ENSP00000419804.1:p.Gly143= | |
| ENST00000488954.1:c.107+6709T>A | ENSP00000418504.1:n.107+6709T>A | |
| ENST00000497011.5:c.429T>A | ENSP00000419505.1:p.Gly143= | |
| NM_000055.2:c.429T>A | NP_000046.1:p.Gly143= | |
| XM_005247685.1:c.552T>A | XP_005247742.1:p.Gly184= | |
| NM_000055.3:c.429T>A | NP_000046.1:p.Gly143= | |
| NR_137635.1:n.159+6709T>A | ||
| NR_137636.1:n.596T>A | ||
| NM_000055.4:c.429T>A MANE Select | NP_000046.1:p.Gly143= | |
| NR_137635.2:n.110+6709T>A | ||
| NR_137636.2:n.547T>A |