Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.19353145G>C , CM000664.2:g.19353145G>C | GRCh38 |
| NC_000002.11:g.19552906G>C , CM000664.1:g.19552906G>C | GRCh37 |
| NC_000002.10:g.19416387G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272223.3:c.661C>G MANE Select | ENSP00000272223.2:p.His221Asp | |
| ENST00000272223.2:c.661C>G | ENSP00000272223.2:p.His221Asp | |
| ENST00000487581.1:n.3768C>G | ||
| NM_145260.2:c.661C>G | NP_660303.1:p.His221Asp | |
| XM_006711942.2:c.661C>G | XP_006712005.1:p.His221Asp | |
| XM_006711942.4:c.661C>G | XP_006712005.1:p.His221Asp | |
| NM_145260.3:c.661C>G MANE Select | NP_660303.1:p.His221Asp |