Linked Data
MyVariant Identifiers:
chr9:g.136131100T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255713T>G , CM000671.2:g.133255713T>G | GRCh38 |
| NC_000009.11:g.136131100T>G , CM000671.1:g.136131100T>G | GRCh37 |
| NC_000009.10:g.135120921T>G | NCBI36 |
| NG_006669.1:g.21955A>C | |
| NG_006669.2:g.24503A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.1047A>C | ||
| ENST00000647353.1:n.54-4561A>C | ||
| ENST00000679909.1:c.28+19449A>C | ENSP00000506089.1:n.28+19449A>C | |
| ENST00000453660.3:n.1029A>C | ||
| ENST00000538324.2:c.1015A>C | ENSP00000483018.1:p.Arg339= | |
| ENST00000611156.4:c.1015A>C | ENSP00000483265.1:p.Arg339= | |
| NM_020469.2:c.1018A>C | NP_065202.2:p.Arg340= | |
| NM_020469.3:c.1018A>C | NP_065202.2:p.Arg340= |