Linked Data
MyVariant Identifiers:
chr12:g.65632488A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65238708A>C , CM000674.2:g.65238708A>C | GRCh38 |
| NC_000012.11:g.65632488A>C , CM000674.1:g.65632488A>C | GRCh37 |
| NC_000012.10:g.63918755A>C | NCBI36 |
| NG_016210.1:g.74138A>C | |
| NG_016210.2:g.74138A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.1815A>C MANE Select | ENSP00000308369.2:p.Ile605= | |
| ENST00000308330.2:c.1815A>C | ENSP00000308369.2:p.Ile605= | |
| NM_001167614.1:c.1812A>C | NP_001161086.1:p.Ile604= | |
| NM_014319.4:c.1815A>C | NP_055134.2:p.Ile605= | |
| NM_014319.5:c.1815A>C MANE Select | NP_055134.2:p.Ile605= | |
| NM_001167614.2:c.1812A>C | NP_001161086.1:p.Ile604= |