Linked Data
MyVariant Identifiers:
chr12:g.65640048C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65246268C>T , CM000674.2:g.65246268C>T | GRCh38 |
| NC_000012.11:g.65640048C>T , CM000674.1:g.65640048C>T | GRCh37 |
| NC_000012.10:g.63926315C>T | NCBI36 |
| NG_016210.1:g.81698C>T | |
| NG_016210.2:g.81698C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.2679C>T MANE Select | ENSP00000308369.2:p.Asn893= | |
| ENST00000308330.2:c.2679C>T | ENSP00000308369.2:p.Asn893= | |
| ENST00000539442.1:n.661C>T | ||
| ENST00000544506.1:n.399C>T | ||
| ENST00000545026.1:n.497C>T | ||
| NM_001167614.1:c.2676C>T | NP_001161086.1:p.Asn892= | |
| NM_014319.4:c.2679C>T | NP_055134.2:p.Asn893= | |
| NM_014319.5:c.2679C>T MANE Select | NP_055134.2:p.Asn893= | |
| NM_001167614.2:c.2676C>T | NP_001161086.1:p.Asn892= |