Linked Data
MyVariant Identifiers:
chr19:g.4817064C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4817052C>G , CM000681.2:g.4817052C>G | GRCh38 |
| NC_000019.9:g.4817064C>G , CM000681.1:g.4817064C>G | GRCh37 |
| NC_000019.8:g.4768064C>G | NCBI36 |
| NG_031998.1:g.19691G>C , LRG_358:g.19691G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1326G>C MANE Select | ENSP00000248244.4:p.Leu442= | |
| ENST00000248244.5:c.1326G>C | ENSP00000248244.4:p.Leu442= | |
| ENST00000621756.1:c.909G>C | ENSP00000479467.1:p.Leu303= | |
| NM_182919.3:c.1326G>C , LRG_358t1:c.1326G>C | NP_891549.1:p.Leu442= | |
| NM_001385678.1:c.1284G>C | NP_001372607.1:p.Leu428= | |
| NM_001385679.1:c.1191G>C | NP_001372608.1:p.Leu397= | |
| NM_001385680.1:c.684G>C | NP_001372609.1:p.Leu228= | |
| NM_182919.4:c.1326G>C MANE Select | NP_891549.1:p.Leu442= |