MyVariant.info:
GRCh37
chr16:g.22268642G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.22257321G>T , CM000678.2:g.22257321G>T | GRCh38 |
| NC_000016.9:g.22268642G>T , CM000678.1:g.22268642G>T | GRCh37 |
| NC_000016.8:g.22176143G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263026.10:c.837G>T MANE Select | ENSP00000263026.5:p.Gly279= | |
| ENST00000263026.9:c.837G>T | ENSP00000263026.5:p.Gly279= | |
| ENST00000568269.5:c.837G>T | ENSP00000456243.1:p.Gly279= | |
| NM_013302.3:c.837G>T | NP_037434.1:p.Gly279= | |
| XR_950786.1:n.1311G>T | ||
| XR_950787.1:n.1311G>T | ||
| XM_017023193.2:c.837G>T | XP_016878682.1:p.Gly279= | |
| XM_017023194.2:c.837G>T | XP_016878683.1:p.Gly279= | |
| XR_001751897.2:n.1311G>T | ||
| XR_950786.3:n.1311G>T | ||
| XR_950787.3:n.1311G>T | ||
| NM_013302.4:c.837G>T | NP_037434.1:p.Gly279= | |
| NM_013302.5:c.837G>T MANE Select | NP_037434.2:p.Gly279= |