Linked Data
MyVariant Identifiers:
chr1:g.154543770T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571294T>C , CM000663.2:g.154571294T>C | GRCh38 |
| NC_000001.10:g.154543770T>C , CM000663.1:g.154543770T>C | GRCh37 |
| NC_000001.9:g.152810394T>C | NCBI36 |
| NG_008027.1:g.8514T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.471T>C MANE Select | ENSP00000357461.3:p.Ile157= | |
| ENST00000636034.1:c.471T>C | ENSP00000489703.1:p.Ile157= | |
| ENST00000637900.1:c.477T>C | ENSP00000490474.1:p.Ile159= | |
| ENST00000368476.3:c.471T>C | ENSP00000357461.3:p.Ile157= | |
| NM_000748.2:c.471T>C | NP_000739.1:p.Ile157= | |
| XM_017000180.2:c.-9-31T>C | XP_016855669.1:n.-9-31T>C | |
| XR_001736952.2:n.723T>C | ||
| NM_000748.3:c.471T>C MANE Select | NP_000739.1:p.Ile157= |