Linked Data
MyVariant Identifiers:
chr22:g.36960875G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36564828G>C , CM000684.2:g.36564828G>C | GRCh38 |
| NC_000022.10:g.36960875G>C , CM000684.1:g.36960875G>C | GRCh37 |
| NC_000022.9:g.35290821G>C | NCBI36 |
| NG_031861.1:g.142816C>G | |
| NG_031861.2:g.143031C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.495C>G MANE Select | ENSP00000300105.6:p.Ser165= | |
| ENST00000300105.6:c.495C>G | ENSP00000300105.6:p.Ser165= | |
| NM_006078.3:c.495C>G | NP_006069.1:p.Ser165= | |
| NM_006078.4:c.495C>G | NP_006069.1:p.Ser165= | |
| XM_017028531.2:c.237C>G | XP_016884020.1:p.Ser79= | |
| NM_001379051.1:c.426C>G | NP_001365980.1:p.Ser142= | |
| NM_006078.5:c.495C>G MANE Select | NP_006069.1:p.Ser165= | |
| NR_166440.1:n.1861C>G |