Linked Data
MyVariant Identifiers:
chr10:g.121429638A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119670126A>C , CM000672.2:g.119670126A>C | GRCh38 |
| NC_000010.10:g.121429638A>C , CM000672.1:g.121429638A>C | GRCh37 |
| NC_000010.9:g.121419628A>C | NCBI36 |
| NG_016125.1:g.23757A>C , LRG_742:g.23757A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369085.8:c.456A>C MANE Select | ENSP00000358081.4:p.Gly152= | |
| ENST00000369085.7:c.456A>C | ENSP00000358081.3:p.Gly152= | |
| ENST00000450186.1:c.282A>C | ENSP00000410036.1:p.Gly94= | |
| NM_004281.3:c.456A>C , LRG_742t1:c.456A>C | NP_004272.2:p.Gly152= | |
| XM_005270287.1:c.456A>C | XP_005270344.1:p.Gly152= | |
| XM_005270287.2:c.456A>C | XP_005270344.1:p.Gly152= | |
| NM_004281.4:c.456A>C MANE Select | NP_004272.2:p.Gly152= |