Linked Data
MyVariant Identifiers:
chr4:g.88533782C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.87612630C>T , CM000666.2:g.87612630C>T | GRCh38 |
| NC_000004.11:g.88533782C>T , CM000666.1:g.88533782C>T | GRCh37 |
| NC_000004.10:g.88752806C>T | NCBI36 |
| NG_011595.1:g.9102C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651931.1:c.444C>T MANE Select | ENSP00000498766.1:p.Ala148= | |
| ENST00000282478.7:c.444C>T | ENSP00000282478.7:p.Ala148= | |
| ENST00000399271.5:c.444C>T | ENSP00000382213.1:p.Ala148= | |
| NM_014208.3:c.444C>T MANE Select | NP_055023.2:p.Ala148= |