Linked Data
MyVariant Identifiers:
chr1:g.147380169T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.147908042T>C , CM000663.2:g.147908042T>C | GRCh38 |
| NC_000001.10:g.147380169T>C , CM000663.1:g.147380169T>C | GRCh37 |
| NC_000001.9:g.145846793T>C | NCBI36 |
| NG_016242.1:g.10224T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369235.2:c.87T>C MANE Select | ENSP00000358238.1:p.Leu29= | |
| ENST00000369235.1:c.87T>C | ENSP00000358238.1:p.Leu29= | |
| NM_005267.4:c.87T>C | NP_005258.2:p.Leu29= | |
| XM_011509416.1:c.87T>C | XP_011507718.1:p.Leu29= | |
| XM_011509417.1:c.87T>C | XP_011507719.1:p.Leu29= | |
| XM_011509417.2:c.87T>C | XP_011507719.1:p.Leu29= | |
| XR_002956281.1:n.1002T>C | ||
| NM_005267.5:c.87T>C MANE Select | NP_005258.2:p.Leu29= |