Linked Data
MyVariant Identifiers:
chr6:g.42689647C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42721909C>G , CM000668.2:g.42721909C>G | GRCh38 |
| NC_000006.11:g.42689647C>G , CM000668.1:g.42689647C>G | GRCh37 |
| NC_000006.10:g.42797625C>G | NCBI36 |
| NG_009176.1:g.5712G>C | |
| NG_009176.2:g.5712G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.426G>C MANE Select | ENSP00000230381.5:p.Arg142= | |
| ENST00000230381.6:c.426G>C | ENSP00000230381.5:p.Arg142= | |
| NM_000322.4:c.426G>C | NP_000313.2:p.Arg142= | |
| XR_427834.2:n.1081G>C | ||
| XR_926295.1:n.1081G>C | ||
| XR_427834.4:n.1131G>C | ||
| XR_926295.3:n.1131G>C | ||
| NM_000322.5:c.426G>C MANE Select | NP_000313.2:p.Arg142= |