Linked Data
MyVariant Identifiers:
chr14:g.75470072C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75003369C>A , CM000676.2:g.75003369C>A | GRCh38 |
| NC_000014.8:g.75470072C>A , CM000676.1:g.75470072C>A | GRCh37 |
| NC_000014.7:g.74539825C>A | NCBI36 |
| NG_013333.1:g.5461C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266126.10:c.258C>A MANE Select | ENSP00000266126.5:p.Leu86= | |
| ENST00000266126.9:c.258C>A | ENSP00000266126.5:p.Leu86= | |
| ENST00000553401.5:c.231C>A | ENSP00000451681.1:p.Leu77= | |
| ENST00000553539.1:n.398C>A | ||
| ENST00000555522.1:n.316C>A | ||
| ENST00000556028.5:c.258C>A | ENSP00000452311.1:p.Leu86= | |
| NM_014239.3:c.258C>A | NP_055054.1:p.Leu86= | |
| NM_014239.4:c.258C>A MANE Select | NP_055054.1:p.Leu86= |