Linked Data
MyVariant Identifiers:
chr2:g.73868252C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73641125C>T , CM000664.2:g.73641125C>T | GRCh38 |
| NC_000002.11:g.73868252C>T , CM000664.1:g.73868252C>T | GRCh37 |
| NC_000002.10:g.73721760C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272425.4:c.504G>A (NAT8) MANE Select | ENSP00000272425.3:p.Gln168= | |
| ENST00000652439.1:n.43C>T (ALMS1P1) | ||
| ENST00000272425.3:c.504G>A (NAT8) | ENSP00000272425.3:p.Gln168= | |
| NM_003960.3:c.504G>A (NAT8) | NP_003951.3:p.Gln168= | |
| NM_003960.4:c.504G>A (NAT8) MANE Select | NP_003951.3:p.Gln168= |