Linked Data
MyVariant Identifiers:
chr6:g.31829142A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31861365A>T , CM000668.2:g.31861365A>T | GRCh38 |
| NC_000006.11:g.31829142A>T , CM000668.1:g.31829142A>T | GRCh37 |
| NC_000006.10:g.31937121A>T | NCBI36 |
| NG_008201.1:g.6568T>A | |
| NG_023058.1:g.22682T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375631.5:c.438T>A MANE Select | ENSP00000364782.4:p.Val146= | |
| ENST00000677054.1:n.1115T>A | ||
| ENST00000677512.1:n.546T>A | ||
| ENST00000678869.1:n.546T>A | ||
| ENST00000375631.4:c.438T>A | ENSP00000364782.4:p.Val146= | |
| ENST00000480384.1:n.467T>A | ||
| ENST00000491768.5:c.438T>A | ENSP00000433127.1:p.Val146= | |
| ENST00000495807.1:n.1006T>A | ||
| NM_000434.3:c.438T>A | NP_000425.1:p.Val146= | |
| NM_000434.4:c.438T>A MANE Select | NP_000425.1:p.Val146= |