Linked Data
MyVariant Identifiers:
chr12:g.6181553C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6072387C>A , CM000674.2:g.6072387C>A | GRCh38 |
| NC_000012.11:g.6181553C>A , CM000674.1:g.6181553C>A | GRCh37 |
| NC_000012.10:g.6051814C>A | NCBI36 |
| NG_009072.1:g.57284G>T | |
| NG_009072.2:g.57284G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.1053G>T MANE Select | ENSP00000261405.5:p.Val351= | |
| ENST00000261405.9:c.1053G>T | ENSP00000261405.5:p.Val351= | |
| ENST00000538635.5:n.420+38128G>T | ||
| NM_000552.3:c.1053G>T | NP_000543.2:p.Val351= | |
| NM_000552.4:c.1053G>T | NP_000543.2:p.Val351= | |
| NM_000552.5:c.1053G>T MANE Select | NP_000543.3:p.Val351= |