MyVariant.info:
GRCh38
chr2:g.21012603C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21012603C>G , CM000664.2:g.21012603C>G | GRCh38 |
| NG_011793.1:g.36471G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673739.2:c.*3571G>C | ENSP00000501110.2:n.*3571G>C | |
| ENST00000673739.1:c.3979G>C | ENSP00000501110.1:n.3979G>C | |
| ENST00000233242.5:c.4265G>C MANE Select | ENSP00000233242.1:p.Cys1422Ser | |
| ENST00000616098.4:c.4265G>C | ENSP00000477990.1:p.Cys1422Ser | |
| NM_000384.2:c.4265G>C | NP_000375.2:p.Cys1422Ser | |
| XM_011532809.1:c.4265G>C | XP_011531111.1:p.Cys1422Ser | |
| NM_000384.3:c.4265G>C MANE Select | NP_000375.3:p.Cys1422Ser |