Linked Data
MyVariant Identifiers:
chr22:g.20230014C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20242491C>G , CM000684.2:g.20242491C>G | GRCh38 |
| NC_000022.10:g.20230014C>G , CM000684.1:g.20230014C>G | GRCh37 |
| NC_000022.9:g.18610014C>G | NCBI36 |
| NG_012176.1:g.30803G>C | |
| NG_012176.2:g.30803G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000043402.8:c.642G>C MANE Select | ENSP00000043402.7:p.Val214= | |
| ENST00000043402.7:c.642G>C | ENSP00000043402.7:p.Val214= | |
| ENST00000416372.5:c.701G>C | ||
| ENST00000425986.1:c.899G>C | ||
| NM_023004.5:c.642G>C | NP_075380.1:p.Val214= | |
| NM_023004.6:c.642G>C MANE Select | NP_075380.1:p.Val214= |