Linked Data
MyVariant Identifiers:
chr1:g.154543788A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571312A>T , CM000663.2:g.154571312A>T | GRCh38 |
| NC_000001.10:g.154543788A>T , CM000663.1:g.154543788A>T | GRCh37 |
| NC_000001.9:g.152810412A>T | NCBI36 |
| NG_008027.1:g.8532A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.489A>T MANE Select | ENSP00000357461.3:p.Pro163= | |
| ENST00000636034.1:c.489A>T | ENSP00000489703.1:p.Pro163= | |
| ENST00000637900.1:c.495A>T | ENSP00000490474.1:p.Pro165= | |
| ENST00000368476.3:c.489A>T | ENSP00000357461.3:p.Pro163= | |
| NM_000748.2:c.489A>T | NP_000739.1:p.Pro163= | |
| XM_017000180.2:c.-9-13A>T | XP_016855669.1:n.-9-13A>T | |
| XR_001736952.2:n.741A>T | ||
| NM_000748.3:c.489A>T MANE Select | NP_000739.1:p.Pro163= |