Linked Data
MyVariant Identifiers:
chr1:g.172634967C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.172665827C>T , CM000663.2:g.172665827C>T | GRCh38 |
| NC_000001.10:g.172634967C>T , CM000663.1:g.172634967C>T | GRCh37 |
| NC_000001.9:g.170901590C>T | NCBI36 |
| NG_007269.1:g.11783C>T , LRG_58:g.11783C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367721.3:c.657C>T MANE Select | ENSP00000356694.2:p.Pro219= | |
| ENST00000340030.4:c.*227C>T | ENSP00000344739.3:n.*227C>T | |
| ENST00000367721.2:c.657C>T | ENSP00000356694.2:p.Pro219= | |
| NM_000639.2:c.657C>T | NP_000630.1:p.Pro219= | |
| NM_001302746.1:c.*227C>T | NP_001289675.1:n.*227C>T | |
| NM_000639.3:c.657C>T MANE Select | NP_000630.1:p.Pro219= | |
| NM_001302746.2:c.*227C>T | NP_001289675.1:n.*227C>T |