Linked Data
MyVariant Identifiers:
chr2:g.208988941G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.208124217G>A , CM000664.2:g.208124217G>A | GRCh38 |
| NC_000002.11:g.208988941G>A , CM000664.1:g.208988941G>A | GRCh37 |
| NC_000002.10:g.208697186G>A | NCBI36 |
| NG_008039.1:g.5373C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264376.5:c.147C>T MANE Select | ENSP00000264376.4:p.Pro49= | |
| ENST00000264376.4:c.147C>T | ENSP00000264376.4:p.Pro49= | |
| NM_006891.3:c.147C>T | NP_008822.2:p.Pro49= | |
| NR_038437.1:n.97+4992G>A | ||
| NM_006891.4:c.147C>T MANE Select | NP_008822.2:p.Pro49= |