Linked Data
MyVariant Identifiers:
chr8:g.19811641A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19954130A>C , CM000670.2:g.19954130A>C | GRCh38 |
| NC_000008.10:g.19811641A>C , CM000670.1:g.19811641A>C | GRCh37 |
| NC_000008.9:g.19855921A>C | NCBI36 |
| NG_008855.1:g.20060A>C | |
| NG_008855.2:g.57414A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.552A>C MANE Select | ENSP00000497642.1:p.Pro184= | |
| ENST00000311322.8:c.552A>C | ENSP00000309757.6:p.Pro184= | |
| ENST00000520959.5:c.324A>C | ENSP00000428496.1:p.Pro108= | |
| NM_000237.2:c.552A>C | NP_000228.1:p.Pro184= | |
| NM_000237.3:c.552A>C MANE Select | NP_000228.1:p.Pro184= |