Linked Data
gnomAD v3:
3-38551539-G-T
gnomAD v4:
3-38551539-G-T
MyVariant Identifiers:
chr3:g.38593030G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.38551539G>T , CM000665.2:g.38551539G>T | GRCh38 |
| NC_000003.11:g.38593030G>T , CM000665.1:g.38593030G>T | GRCh37 |
| NC_000003.10:g.38568034G>T | NCBI36 |
| NG_008934.1:g.103134C>A , LRG_289:g.103134C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327956.7:c.4830C>A | ENSP00000333674.7:p.Ile1610= | |
| ENST00000333535.9:c.4833C>A | ENSP00000328968.4:p.Ile1611= | |
| ENST00000413689.6:c.4833C>A MANE Plus Clinical | ENSP00000410257.1:p.Ile1611= | |
| ENST00000423572.7:c.4830C>A MANE Select | ENSP00000398266.2:p.Ile1610= | |
| ENST00000333535.8:c.4833C>A | ENSP00000328968.4:p.Ile1611= | |
| ENST00000413689.5:c.4833C>A | ENSP00000410257.1:p.Ile1611= | |
| ENST00000414099.6:c.4779C>A | ENSP00000398962.2:p.Ile1593= | |
| ENST00000423572.6:c.4830C>A | ENSP00000398266.2:p.Ile1610= | |
| ENST00000425664.5:c.4779C>A | ENSP00000416634.1:p.Ile1593= | |
| ENST00000449557.6:c.4671C>A | ENSP00000413996.2:p.Ile1557= | |
| ENST00000450102.6:c.4671C>A | ENSP00000403355.2:p.Ile1557= | |
| ENST00000451551.6:c.4671C>A | ENSP00000388797.2:p.Ile1557= | |
| ENST00000455624.6:c.4734C>A | ENSP00000399524.2:p.Ile1578= | |
| NM_000335.4:c.4830C>A , LRG_289t2:c.4830C>A | NP_000326.2:p.Ile1610= | |
| NM_001099404.1:c.4833C>A , LRG_289t3:c.4833C>A | NP_001092874.1:p.Ile1611= | |
| NM_001099405.1:c.4779C>A | NP_001092875.1:p.Ile1593= | |
| NM_001160160.1:c.4734C>A | NP_001153632.1:p.Ile1578= | |
| NM_001160161.1:c.4671C>A | NP_001153633.1:p.Ile1557= | |
| NM_198056.2:c.4833C>A , LRG_289t1:c.4833C>A | NP_932173.1:p.Ile1611= | |
| XM_006713282.2:c.4833C>A | XP_006713345.1:p.Ile1611= | |
| XM_011533991.1:c.4830C>A | XP_011532293.1:p.Ile1610= | |
| XM_011533992.1:c.4704C>A | XP_011532294.1:p.Ile1568= | |
| NM_001354701.1:c.4776C>A | NP_001341630.1:p.Ile1592= | |
| XM_011533991.2:c.4830C>A | XP_011532293.1:p.Ile1610= | |
| XM_017007017.1:c.4671C>A | XP_016862506.1:p.Ile1557= | |
| NM_000335.5:c.4830C>A MANE Select | NP_000326.2:p.Ile1610= | |
| NM_001160160.2:c.4734C>A | NP_001153632.1:p.Ile1578= | |
| NM_001354701.2:c.4776C>A | NP_001341630.1:p.Ile1592= | |
| NM_001099404.2:c.4833C>A MANE Plus Clinical | NP_001092874.1:p.Ile1611= | |
| NM_001099405.2:c.4779C>A | NP_001092875.1:p.Ile1593= | |
| NM_001160161.2:c.4671C>A | NP_001153633.1:p.Ile1557= | |
| NM_198056.3:c.4833C>A | NP_932173.1:p.Ile1611= |