Linked Data
MyVariant Identifiers:
chr2:g.241808709T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869292T>C , CM000664.2:g.240869292T>C | GRCh38 |
| NC_000002.11:g.241808709T>C , CM000664.1:g.241808709T>C | GRCh37 |
| NC_000002.10:g.241457382T>C | NCBI36 |
| NG_008005.1:g.5548T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.288T>C MANE Select | ENSP00000302620.3:p.Pro96= | |
| ENST00000307503.3:c.288T>C | ENSP00000302620.3:p.Pro96= | |
| ENST00000472436.1:n.308T>C | ||
| NM_000030.2:c.288T>C | NP_000021.1:p.Pro96= | |
| XR_924060.1:n.405+941A>G | ||
| NM_000030.3:c.288T>C MANE Select | NP_000021.1:p.Pro96= |