Linked Data
MyVariant Identifiers:
chr16:g.67976668C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67942765C>T , CM000678.2:g.67942765C>T | GRCh38 |
| NC_000016.9:g.67976668C>T , CM000678.1:g.67976668C>T | GRCh37 |
| NC_000016.8:g.66534169C>T | NCBI36 |
| NG_009778.1:g.6348G>A | |
| NG_033098.1:g.30930G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.429G>A MANE Select | ENSP00000264005.5:p.Gly143= | |
| ENST00000264005.9:c.429G>A | ENSP00000264005.5:p.Gly143= | |
| ENST00000570369.5:c.155+96G>A | ||
| ENST00000570980.1:c.213G>A | ENSP00000464651.1:p.Gly71= | |
| ENST00000573538.5:c.72G>A | ENSP00000463220.1:p.Gly24= | |
| ENST00000573846.1:n.43G>A | ||
| ENST00000575277.1:n.207G>A | ||
| ENST00000575467.5:c.*124G>A | ENSP00000460653.1:n.*124G>A | |
| NM_000229.1:c.429G>A | NP_000220.1:p.Gly143= | |
| NM_000229.2:c.429G>A MANE Select | NP_000220.1:p.Gly143= |