Linked Data
MyVariant Identifiers:
chr19:g.2251647C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2251648C>T , CM000681.2:g.2251648C>T | GRCh38 |
| NC_000019.9:g.2251647C>T , CM000681.1:g.2251647C>T | GRCh37 |
| NC_000019.8:g.2202647C>T | NCBI36 |
| NG_012190.1:g.7535C>T | |
| NG_032853.1:g.9776G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221496.5:c.1374C>T MANE Select | ENSP00000221496.2:p.Ala458= | |
| ENST00000221496.4:c.1374C>T | ENSP00000221496.2:p.Ala458= | |
| NM_000479.3:c.1374C>T | NP_000470.2:p.Ala458= | |
| NM_000479.4:c.1374C>T | NP_000470.2:p.Ala458= | |
| NM_000479.5:c.1374C>T MANE Select | NP_000470.3:p.Ala458= |