Linked Data
MyVariant Identifiers:
chr6:g.31829133T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31861356T>C , CM000668.2:g.31861356T>C | GRCh38 |
| NC_000006.11:g.31829133T>C , CM000668.1:g.31829133T>C | GRCh37 |
| NC_000006.10:g.31937112T>C | NCBI36 |
| NG_008201.1:g.6577A>G | |
| NG_023058.1:g.22691A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375631.5:c.447A>G MANE Select | ENSP00000364782.4:p.Gly149= | |
| ENST00000677054.1:n.1124A>G | ||
| ENST00000677512.1:n.555A>G | ||
| ENST00000678869.1:n.555A>G | ||
| ENST00000375631.4:c.447A>G | ENSP00000364782.4:p.Gly149= | |
| ENST00000480384.1:n.476A>G | ||
| ENST00000491768.5:c.447A>G | ENSP00000433127.1:p.Gly149= | |
| ENST00000495807.1:n.1015A>G | ||
| NM_000434.3:c.447A>G | NP_000425.1:p.Gly149= | |
| NM_000434.4:c.447A>G MANE Select | NP_000425.1:p.Gly149= |