Linked Data
MyVariant Identifiers:
chr1:g.215901576C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215728234C>T , CM000663.2:g.215728234C>T | GRCh38 |
| NC_000001.10:g.215901576C>T , CM000663.1:g.215901576C>T | GRCh37 |
| NC_000001.9:g.213968199C>T | NCBI36 |
| NG_009497.1:g.700163G>A | |
| NG_009497.2:g.700215G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.11862G>A MANE Select | ENSP00000305941.3:p.Leu3954= | |
| ENST00000674083.1:c.11862G>A | ENSP00000501296.1:p.Leu3954= | |
| ENST00000307340.7:c.11862G>A | ENSP00000305941.3:p.Leu3954= | |
| NM_206933.2:c.11862G>A | NP_996816.2:p.Leu3954= | |
| NM_206933.3:c.11862G>A | NP_996816.2:p.Leu3954= | |
| NM_206933.4:c.11862G>A MANE Select | NP_996816.3:p.Leu3954= |