Linked Data
MyVariant Identifiers:
chr2:g.74372413C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.74145286C>A , CM000664.2:g.74145286C>A | GRCh38 |
| NC_000002.11:g.74372413C>A , CM000664.1:g.74372413C>A | GRCh37 |
| NC_000002.10:g.74225921C>A | NCBI36 |
| NG_031910.1:g.7627G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327428.10:c.72G>T MANE Select | ENSP00000331369.5:p.Arg24= | |
| ENST00000295326.4:c.72G>T | ENSP00000295326.4:p.Arg24= | |
| ENST00000327428.9:c.72G>T | ENSP00000331369.5:p.Arg24= | |
| ENST00000469676.1:n.1095G>T | ||
| ENST00000477685.5:n.223G>T | ||
| ENST00000484655.1:n.2627G>T | ||
| NM_001035505.1:c.72G>T | NP_001030582.1:p.Arg24= | |
| NM_212552.2:c.72G>T | NP_997717.2:p.Arg24= | |
| NM_212552.3:c.72G>T MANE Select | NP_997717.2:p.Arg24= | |
| NM_001035505.2:c.72G>T | NP_001030582.1:p.Arg24= |