Linked Data
MyVariant Identifiers:
chr5:g.1213664C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1213549C>T , CM000667.2:g.1213549C>T | GRCh38 |
| NC_000005.9:g.1213664C>T , CM000667.1:g.1213664C>T | GRCh37 |
| NC_000005.8:g.1266664C>T | NCBI36 |
| NG_008282.1:g.16955C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304460.11:c.750C>T MANE Select | ENSP00000305302.10:p.Gly250= | |
| ENST00000304460.10:c.750C>T | ENSP00000305302.10:p.Gly250= | |
| ENST00000515652.5:c.658C>T | ENSP00000425701.1:p.His220Tyr | |
| NM_001003841.2:c.750C>T | NP_001003841.1:p.Gly250= | |
| NM_001003841.3:c.750C>T MANE Select | NP_001003841.1:p.Gly250= |