Linked Data
MyVariant Identifiers:
chr19:g.6714062A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714051A>C , CM000681.2:g.6714051A>C | GRCh38 |
| NC_000019.9:g.6714062A>C , CM000681.1:g.6714062A>C | GRCh37 |
| NC_000019.8:g.6665062A>C | NCBI36 |
| NG_009557.1:g.11601T>G , LRG_27:g.11601T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.591T>G | ENSP00000512083.1:p.Pro197= | |
| ENST00000245907.11:c.714T>G MANE Select | ENSP00000245907.4:p.Pro238= | |
| ENST00000245907.10:c.714T>G | ENSP00000245907.4:p.Pro238= | |
| ENST00000595577.1:n.218T>G | ||
| NM_000064.3:c.714T>G | NP_000055.2:p.Pro238= | |
| NM_000064.4:c.714T>G MANE Select | NP_000055.2:p.Pro238= |