Linked Data
MyVariant Identifiers:
chr5:g.134367032G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135031342G>T , CM000667.2:g.135031342G>T | GRCh38 |
| NC_000005.9:g.134367032G>T , CM000667.1:g.134367032G>T | GRCh37 |
| NC_000005.8:g.134394931G>T | NCBI36 |
| NG_012114.1:g.7933C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.336C>A MANE Select | ENSP00000265340.6:p.Arg112= | |
| ENST00000265340.11:c.336C>A | ENSP00000265340.6:p.Arg112= | |
| ENST00000502676.1:c.336C>A | ENSP00000423624.1:p.Arg112= | |
| ENST00000503586.1:c.458C>A | ||
| ENST00000504936.1:n.669C>A | ||
| ENST00000506438.5:c.336C>A | ENSP00000427542.1:p.Arg112= | |
| ENST00000507253.5:c.336C>A | ENSP00000422908.1:p.Arg112= | |
| NM_002653.4:c.336C>A | NP_002644.4:p.Arg112= | |
| NM_002653.5:c.336C>A MANE Select | NP_002644.4:p.Arg112= |