Linked Data
MyVariant Identifiers:
chr19:g.4816644T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816632T>G , CM000681.2:g.4816632T>G | GRCh38 |
| NC_000019.9:g.4816644T>G , CM000681.1:g.4816644T>G | GRCh37 |
| NC_000019.8:g.4767644T>G | NCBI36 |
| NG_031998.1:g.20111A>C , LRG_358:g.20111A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1746A>C MANE Select | ENSP00000248244.4:p.Ala582= | |
| ENST00000248244.5:c.1746A>C | ENSP00000248244.4:p.Ala582= | |
| ENST00000621756.1:c.1329A>C | ENSP00000479467.1:p.Ala443= | |
| NM_182919.3:c.1746A>C , LRG_358t1:c.1746A>C | NP_891549.1:p.Ala582= | |
| NM_001385678.1:c.1704A>C | NP_001372607.1:p.Ala568= | |
| NM_001385679.1:c.1611A>C | NP_001372608.1:p.Ala537= | |
| NM_001385680.1:c.1104A>C | NP_001372609.1:p.Ala368= | |
| NM_182919.4:c.1746A>C MANE Select | NP_891549.1:p.Ala582= |