Linked Data
gnomAD v3:
1-40784204-C-T
gnomAD v4:
1-40784204-C-T
MyVariant Identifiers:
chr1:g.41249876C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40784204C>T , CM000663.2:g.40784204C>T | GRCh38 |
| NC_000001.10:g.41249876C>T , CM000663.1:g.41249876C>T | GRCh37 |
| NC_000001.9:g.41022463C>T | NCBI36 |
| NG_008139.1:g.5193C>T | |
| NG_008139.2:g.5193C>T | |
| NG_008139.3:g.5418C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347132.10:c.111C>T MANE Select | ENSP00000262916.6:p.Gly37= | |
| ENST00000347132.9:c.111C>T | ENSP00000262916.6:p.Gly37= | |
| ENST00000509682.6:c.111C>T | ENSP00000423756.2:p.Gly37= | |
| NM_004700.3:c.111C>T | NP_004691.2:p.Gly37= | |
| NM_172163.2:c.111C>T | NP_751895.1:p.Gly37= | |
| XM_011542417.1:c.111C>T | XP_011540719.1:p.Gly37= | |
| XM_011542418.1:c.111C>T | XP_011540720.1:p.Gly37= | |
| XM_011542419.1:c.111C>T | XP_011540721.1:p.Gly37= | |
| XM_011542420.1:c.111C>T | XP_011540722.1:p.Gly37= | |
| XR_946798.1:n.117C>T | ||
| XR_946799.1:n.117C>T | ||
| XR_946800.1:n.117C>T | ||
| NM_004700.4:c.111C>T MANE Select | NP_004691.2:p.Gly37= | |
| NM_172163.3:c.111C>T | NP_751895.1:p.Gly37= |