Linked Data
MyVariant Identifiers:
chr3:g.49160742G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49123309G>T , CM000665.2:g.49123309G>T | GRCh38 |
| NC_000003.11:g.49160742G>T , CM000665.1:g.49160742G>T | GRCh37 |
| NC_000003.10:g.49135746G>T | NCBI36 |
| NG_008094.1:g.14858C>A | |
| NG_054716.1:g.2630C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305544.9:c.4047C>A MANE Select | ENSP00000307156.4:p.Thr1349= | |
| ENST00000305544.8:c.4047C>A | ENSP00000307156.4:p.Thr1349= | |
| ENST00000418109.5:c.4047C>A | ENSP00000388325.1:p.Thr1349= | |
| ENST00000469665.1:n.277C>A | ||
| NM_002292.3:c.4047C>A | NP_002283.3:p.Thr1349= | |
| XM_005265127.3:c.4047C>A | XP_005265184.1:p.Thr1349= | |
| XM_005265127.4:c.4047C>A | XP_005265184.1:p.Thr1349= | |
| NM_002292.4:c.4047C>A MANE Select | NP_002283.3:p.Thr1349= |