Linked Data
MyVariant Identifiers:
chr8:g.18257564C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400054C>T , CM000670.2:g.18400054C>T | GRCh38 |
| NC_000008.10:g.18257564C>T , CM000670.1:g.18257564C>T | GRCh37 |
| NC_000008.9:g.18301844C>T | NCBI36 |
| NG_012246.1:g.13810C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.51C>T MANE Select | ENSP00000286479.3:p.Asn17= | |
| ENST00000286479.3:c.51C>T | ENSP00000286479.3:p.Asn17= | |
| ENST00000520116.1:c.-57-283C>T | ENSP00000428416.1:n.-57-283C>T | |
| NM_000015.2:c.51C>T | NP_000006.2:p.Asn17= | |
| XM_011544358.1:c.51C>T | XP_011542660.1:p.Asn17= | |
| XM_017012938.1:c.51C>T | XP_016868427.1:p.Asn17= | |
| NM_000015.3:c.51C>T MANE Select | NP_000006.2:p.Asn17= |