Linked Data
MyVariant Identifiers:
chr14:g.68191895C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.67725178C>T , CM000676.2:g.67725178C>T | GRCh38 |
| NC_000014.8:g.68191895C>T , CM000676.1:g.68191895C>T | GRCh37 |
| NC_000014.7:g.67261648C>T | NCBI36 |
| NG_008321.1:g.28293C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551171.6:c.267C>T (RDH12) MANE Select | ENSP00000449079.1:p.Asn89= | |
| ENST00000267502.3:c.267C>T (RDH12) | ENSP00000267502.3:p.Asn89= | |
| ENST00000551171.5:c.267C>T (RDH12) | ENSP00000449079.1:p.Asn89= | |
| NM_152443.2:c.267C>T (RDH12) | NP_689656.2:p.Asn89= | |
| XM_017020925.2:c.1313-10017C>T (GPHN) | XP_016876414.1:n.1313-10017C>T | |
| NM_152443.3:c.267C>T (RDH12) MANE Select | NP_689656.2:p.Asn89= |