Linked Data
MyVariant Identifiers:
chr6:g.42689572G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42721834G>T , CM000668.2:g.42721834G>T | GRCh38 |
| NC_000006.11:g.42689572G>T , CM000668.1:g.42689572G>T | GRCh37 |
| NC_000006.10:g.42797550G>T | NCBI36 |
| NG_009176.1:g.5787C>A | |
| NG_009176.2:g.5787C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.501C>A MANE Select | ENSP00000230381.5:p.Gly167= | |
| ENST00000230381.6:c.501C>A | ENSP00000230381.5:p.Gly167= | |
| NM_000322.4:c.501C>A | NP_000313.2:p.Gly167= | |
| XR_427834.2:n.1156C>A | ||
| XR_926295.1:n.1156C>A | ||
| XR_427834.4:n.1206C>A | ||
| XR_926295.3:n.1206C>A | ||
| NM_000322.5:c.501C>A MANE Select | NP_000313.2:p.Gly167= |