Linked Data
MyVariant Identifiers:
chr2:g.241818196C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240878779C>T , CM000664.2:g.240878779C>T | GRCh38 |
| NC_000002.11:g.241818196C>T , CM000664.1:g.241818196C>T | GRCh37 |
| NC_000002.10:g.241466869C>T | NCBI36 |
| NG_008005.1:g.15035C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.1137C>T MANE Select | ENSP00000302620.3:p.Ala379= | |
| ENST00000307503.3:c.1137C>T | ENSP00000302620.3:p.Ala379= | |
| ENST00000470255.1:n.915C>T | ||
| NM_000030.2:c.1137C>T | NP_000021.1:p.Ala379= | |
| NM_000030.3:c.1137C>T MANE Select | NP_000021.1:p.Ala379= |