Linked Data
MyVariant Identifiers:
chr1:g.169511157G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169541919G>A , CM000663.2:g.169541919G>A | GRCh38 |
| NC_000001.10:g.169511157G>A , CM000663.1:g.169511157G>A | GRCh37 |
| NC_000001.9:g.167777781G>A | NCBI36 |
| NG_011806.1:g.49613C>T , LRG_553:g.49613C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.3171C>T MANE Select | ENSP00000356771.3:p.Asn1057= | |
| ENST00000367796.3:c.3186C>T | ENSP00000356770.3:p.Asn1062= | |
| ENST00000367797.7:c.3171C>T | ENSP00000356771.3:p.Asn1057= | |
| NM_000130.4:c.3171C>T , LRG_553t1:c.3171C>T | NP_000121.2:p.Asn1057= | |
| XM_017000660.2:c.2760C>T | XP_016856149.1:p.Asn920= | |
| NM_000130.5:c.3171C>T MANE Select | NP_000121.2:p.Asn1057= |