Linked Data
MyVariant Identifiers:
chr1:g.204124204T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204155076T>C , CM000663.2:g.204155076T>C | GRCh38 |
| NC_000001.10:g.204124204T>C , CM000663.1:g.204124204T>C | GRCh37 |
| NC_000001.9:g.202390827T>C | NCBI36 |
| NG_012122.1:g.16262A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272190.9:c.1161A>G MANE Select | ENSP00000272190.8:p.Arg387= | |
| ENST00000638118.1:c.1047A>G | ENSP00000490307.1:p.Arg349= | |
| ENST00000272190.8:c.1161A>G | ENSP00000272190.8:p.Arg387= | |
| NM_000537.3:c.1161A>G | NP_000528.1:p.Arg387= | |
| NM_000537.4:c.1161A>G MANE Select | NP_000528.1:p.Arg387= |