Linked Data
MyVariant Identifiers:
chr2:g.241808748G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869331G>T , CM000664.2:g.240869331G>T | GRCh38 |
| NC_000002.11:g.241808748G>T , CM000664.1:g.241808748G>T | GRCh37 |
| NC_000002.10:g.241457421G>T | NCBI36 |
| NG_008005.1:g.5587G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.327G>T MANE Select | ENSP00000302620.3:p.Gly109= | |
| ENST00000307503.3:c.327G>T | ENSP00000302620.3:p.Gly109= | |
| ENST00000472436.1:n.347G>T | ||
| NM_000030.2:c.327G>T | NP_000021.1:p.Gly109= | |
| XR_924060.1:n.405+902C>A | ||
| NM_000030.3:c.327G>T MANE Select | NP_000021.1:p.Gly109= |