Linked Data
MyVariant Identifiers:
chr3:g.49160703T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49123270T>C , CM000665.2:g.49123270T>C | GRCh38 |
| NC_000003.11:g.49160703T>C , CM000665.1:g.49160703T>C | GRCh37 |
| NC_000003.10:g.49135707T>C | NCBI36 |
| NG_008094.1:g.14897A>G | |
| NG_054716.1:g.2669A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305544.9:c.4086A>G MANE Select | ENSP00000307156.4:p.Ala1362= | |
| ENST00000305544.8:c.4086A>G | ENSP00000307156.4:p.Ala1362= | |
| ENST00000418109.5:c.4086A>G | ENSP00000388325.1:p.Ala1362= | |
| ENST00000469665.1:n.316A>G | ||
| NM_002292.3:c.4086A>G | NP_002283.3:p.Ala1362= | |
| XM_005265127.3:c.4086A>G | XP_005265184.1:p.Ala1362= | |
| XM_005265127.4:c.4086A>G | XP_005265184.1:p.Ala1362= | |
| NM_002292.4:c.4086A>G MANE Select | NP_002283.3:p.Ala1362= |