Linked Data
MyVariant Identifiers:
chr1:g.20944965G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.20618472G>C , CM000663.2:g.20618472G>C | GRCh38 |
| NC_000001.10:g.20944965G>C , CM000663.1:g.20944965G>C | GRCh37 |
| NC_000001.9:g.20817552G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375071.4:c.345G>C MANE Select | ENSP00000364212.3:p.Val115= | |
| ENST00000375071.3:c.345G>C | ENSP00000364212.3:p.Val115= | |
| ENST00000461985.1:n.331G>C | ||
| NM_001785.2:c.345G>C | NP_001776.1:p.Val115= | |
| NM_001785.3:c.345G>C MANE Select | NP_001776.1:p.Val115= |