Linked Data
MyVariant Identifiers:
chr17:g.7989350T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8086032T>G , CM000679.2:g.8086032T>G | GRCh38 |
| NC_000017.10:g.7989350T>G , CM000679.1:g.7989350T>G | GRCh37 |
| NC_000017.9:g.7930075T>G | NCBI36 |
| NG_007099.1:g.6672A>C | |
| NG_007099.2:g.6685A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.336A>C MANE Select | ENSP00000497784.1:p.Ala112= | |
| ENST00000319144.4:c.336A>C | ENSP00000315167.4:p.Ala112= | |
| NM_001139.2:c.336A>C | NP_001130.1:p.Ala112= | |
| NM_001139.3:c.336A>C MANE Select | NP_001130.1:p.Ala112= |