Linked Data
MyVariant Identifiers:
chr19:g.6713439A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713428A>C , CM000681.2:g.6713428A>C | GRCh38 |
| NC_000019.9:g.6713439A>C , CM000681.1:g.6713439A>C | GRCh37 |
| NC_000019.8:g.6664439A>C | NCBI36 |
| NG_009557.1:g.12224T>G , LRG_27:g.12224T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.732T>G | ENSP00000512083.1:p.Pro244= | |
| ENST00000695692.1:n.179T>G | ||
| ENST00000245907.11:c.855T>G MANE Select | ENSP00000245907.4:p.Pro285= | |
| ENST00000245907.10:c.855T>G | ENSP00000245907.4:p.Pro285= | |
| ENST00000595577.1:n.359T>G | ||
| ENST00000597442.5:n.105T>G | ||
| NM_000064.3:c.855T>G | NP_000055.2:p.Pro285= | |
| NM_000064.4:c.855T>G MANE Select | NP_000055.2:p.Pro285= |