Linked Data
MyVariant Identifiers:
chr6:g.31827523G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31859746G>C , CM000668.2:g.31859746G>C | GRCh38 |
| NC_000006.11:g.31827523G>C , CM000668.1:g.31827523G>C | GRCh37 |
| NC_000006.10:g.31935502G>C | NCBI36 |
| NG_008201.1:g.8187C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375631.5:c.1221C>G MANE Select | ENSP00000364782.4:p.Ala407= | |
| ENST00000677054.1:n.2560C>G | ||
| ENST00000677512.1:n.1498C>G | ||
| ENST00000678869.1:n.1809C>G | ||
| ENST00000375631.4:c.1221C>G | ENSP00000364782.4:p.Ala407= | |
| ENST00000480384.1:n.1520C>G | ||
| ENST00000491768.5:c.*331C>G | ENSP00000433127.1:n.*331C>G | |
| ENST00000495807.1:n.2529C>G | ||
| NM_000434.3:c.1221C>G | NP_000425.1:p.Ala407= | |
| NM_000434.4:c.1221C>G MANE Select | NP_000425.1:p.Ala407= |