Linked Data
MyVariant Identifiers:
chr7:g.21920481C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21880863C>T , CM000669.2:g.21880863C>T | GRCh38 |
| NC_000007.13:g.21920481C>T , CM000669.1:g.21920481C>T | GRCh37 |
| NC_000007.12:g.21887006C>T | NCBI36 |
| NG_012886.2:g.342649C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.12357C>T MANE Select | ENSP00000475939.1:p.Val4119= | |
| ENST00000328843.10:c.12378C>T | ENSP00000330671.7:p.Val4126= | |
| ENST00000409508.7:c.12357C>T | ENSP00000475939.1:p.Val4119= | |
| ENST00000620169.4:c.12378C>T | ENSP00000481693.1:p.Val4126= | |
| NM_001277115.1:c.12357C>T | NP_001264044.1:p.Val4119= | |
| NM_001277115.2:c.12357C>T MANE Select | NP_001264044.1:p.Val4119= |