Linked Data
MyVariant Identifiers:
chr1:g.204159681G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190553G>T , CM000663.2:g.204190553G>T | GRCh38 |
| NC_000001.10:g.204159681G>T , CM000663.1:g.204159681G>T | GRCh37 |
| NC_000001.9:g.202426304G>T | NCBI36 |
| NG_032151.1:g.10939C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.348C>A MANE Select | ENSP00000356162.4:p.Ser116= | |
| ENST00000367194.4:c.348C>A | ENSP00000356162.4:p.Ser116= | |
| ENST00000625357.1:c.348C>A | ENSP00000485957.1:p.Ser116= | |
| NM_002256.3:c.348C>A | NP_002247.3:p.Ser116= | |
| XM_011509525.1:c.348C>A | XP_011507827.1:p.Ser116= | |
| NM_002256.4:c.348C>A MANE Select | NP_002247.3:p.Ser116= |