MyVariant.info:
GRCh37
chr1:g.155230131C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155260340C>G , CM000663.2:g.155260340C>G | GRCh38 |
| NC_000001.10:g.155230131C>G , CM000663.1:g.155230131C>G | GRCh37 |
| NC_000001.9:g.153496755C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302631.8:c.378G>C MANE Select | ENSP00000307275.3:p.Gly126= | |
| ENST00000302631.7:c.378G>C | ENSP00000307275.3:p.Gly126= | |
| ENST00000355379.3:c.300G>C | ENSP00000347540.3:p.Gly100= | |
| ENST00000462151.5:n.446G>C | ||
| ENST00000465312.5:n.376G>C | ||
| ENST00000472397.5:n.111G>C | ||
| ENST00000490999.5:n.313G>C | ||
| ENST00000497470.1:n.706G>C | ||
| NM_005698.3:c.378G>C | NP_005689.2:p.Gly126= | |
| NM_052837.2:c.300G>C | NP_443069.1:p.Gly100= | |
| XM_006711105.2:c.378G>C | XP_006711168.1:p.Gly126= | |
| XM_006711106.2:c.177G>C | XP_006711169.1:p.Gly59= | |
| XM_006711107.2:c.177G>C | XP_006711170.1:p.Gly59= | |
| NM_005698.4:c.378G>C MANE Select | NP_005689.2:p.Gly126= | |
| NM_052837.3:c.300G>C | NP_443069.1:p.Gly100= |