Linked Data
MyVariant Identifiers:
chr1:g.215955417A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215782075A>T , CM000663.2:g.215782075A>T | GRCh38 |
| NC_000001.10:g.215955417A>T , CM000663.1:g.215955417A>T | GRCh37 |
| NC_000001.9:g.214022040A>T | NCBI36 |
| NG_009497.1:g.646322T>A | |
| NG_009497.2:g.646374T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.10707T>A MANE Select | ENSP00000305941.3:p.Ala3569= | |
| ENST00000674083.1:c.10707T>A | ENSP00000501296.1:p.Ala3569= | |
| ENST00000307340.7:c.10707T>A | ENSP00000305941.3:p.Ala3569= | |
| NM_206933.2:c.10707T>A | NP_996816.2:p.Ala3569= | |
| NM_206933.3:c.10707T>A | NP_996816.2:p.Ala3569= | |
| NM_206933.4:c.10707T>A MANE Select | NP_996816.3:p.Ala3569= |