Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137199188C>G , CM000671.2:g.137199188C>G | GRCh38 |
| NC_000009.11:g.140093640C>G , CM000671.1:g.140093640C>G | GRCh37 |
| NC_000009.10:g.139213461C>G | NCBI36 |
| NG_027801.1:g.6524G>C | |
| NG_027801.2:g.10006G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409012.6:c.1524G>C MANE Select | ENSP00000387100.4:p.Lys508Asn | |
| ENST00000333046.8:c.918G>C | ENSP00000327617.4:p.Lys306Asn | |
| ENST00000409012.4:c.1524G>C | ENSP00000387100.4:p.Lys508Asn | |
| ENST00000541945.1:n.90+4916G>C | ||
| NM_001128228.2:c.1524G>C | NP_001121700.2:p.Lys508Asn | |
| NM_001128228.3:c.1524G>C MANE Select | NP_001121700.2:p.Lys508Asn |