Linked Data
MyVariant Identifiers:
chr12:g.65632305T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65238525T>A , CM000674.2:g.65238525T>A | GRCh38 |
| NC_000012.11:g.65632305T>A , CM000674.1:g.65632305T>A | GRCh37 |
| NC_000012.10:g.63918572T>A | NCBI36 |
| NG_016210.1:g.73955T>A | |
| NG_016210.2:g.73955T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.1719T>A MANE Select | ENSP00000308369.2:p.Gly573= | |
| ENST00000308330.2:c.1719T>A | ENSP00000308369.2:p.Gly573= | |
| NM_001167614.1:c.1716T>A | NP_001161086.1:p.Gly572= | |
| NM_014319.4:c.1719T>A | NP_055134.2:p.Gly573= | |
| NM_014319.5:c.1719T>A MANE Select | NP_055134.2:p.Gly573= | |
| NM_001167614.2:c.1716T>A | NP_001161086.1:p.Gly572= |