MyVariant.info:
GRCh37
chr6:g.31604044T>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31636267T>C , CM000668.2:g.31636267T>C | GRCh38 |
| NC_000006.11:g.31604044T>C , CM000668.1:g.31604044T>C | GRCh37 |
| NC_000006.10:g.31712023T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376033.3:c.5683T>C MANE Select | ENSP00000365201.2:p.Leu1895= | |
| ENST00000376007.8:c.5683T>C | ENSP00000365175.4:p.Leu1895= | |
| ENST00000376033.2:c.5683T>C | ENSP00000365201.2:p.Leu1895= | |
| ENST00000487839.1:n.617T>C | ||
| ENST00000492691.5:n.21T>C | ||
| NM_004638.3:c.5683T>C | NP_004629.3:p.Leu1895= | |
| NM_080686.2:c.5683T>C | NP_542417.2:p.Leu1895= | |
| XM_011514890.1:c.5683T>C | XP_011513192.1:p.Leu1895= | |
| XM_017011274.1:c.5683T>C | XP_016866763.1:p.Leu1895= | |
| NM_004638.4:c.5683T>C MANE Select | NP_004629.3:p.Leu1895= | |
| NM_080686.3:c.5683T>C | NP_542417.2:p.Leu1895= |