Linked Data
MyVariant Identifiers:
chr1:g.215844560C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215671218C>T , CM000663.2:g.215671218C>T | GRCh38 |
| NC_000001.10:g.215844560C>T , CM000663.1:g.215844560C>T | GRCh37 |
| NC_000001.9:g.213911183C>T | NCBI36 |
| NG_009497.1:g.757179G>A | |
| NG_009497.2:g.757231G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.13887G>A MANE Select | ENSP00000305941.3:p.Glu4629= | |
| ENST00000674083.1:c.13887G>A | ENSP00000501296.1:p.Glu4629= | |
| ENST00000307340.7:c.13887G>A | ENSP00000305941.3:p.Glu4629= | |
| NM_206933.2:c.13887G>A | NP_996816.2:p.Glu4629= | |
| NM_206933.3:c.13887G>A | NP_996816.2:p.Glu4629= | |
| NM_206933.4:c.13887G>A MANE Select | NP_996816.3:p.Glu4629= |