Linked Data
MyVariant Identifiers:
chr2:g.73118477T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.72891348T>C , CM000664.2:g.72891348T>C | GRCh38 |
| NC_000002.11:g.73118477T>C , CM000664.1:g.73118477T>C | GRCh37 |
| NC_000002.10:g.72971985T>C | NCBI36 |
| NG_008234.1:g.8966T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000234454.6:c.597T>C MANE Select | ENSP00000234454.5:p.Gly199= | |
| ENST00000234454.5:c.597T>C | ENSP00000234454.5:p.Gly199= | |
| ENST00000498749.1:n.542T>C | ||
| NM_003124.4:c.597T>C | NP_003115.1:p.Gly199= | |
| NM_003124.5:c.597T>C MANE Select | NP_003115.1:p.Gly199= |