Linked Data
MyVariant Identifiers:
chr14:g.61115437C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60648719C>T , CM000676.2:g.60648719C>T | GRCh38 |
| NC_000014.8:g.61115437C>T , CM000676.1:g.61115437C>T | GRCh37 |
| NC_000014.7:g.60185190C>T | NCBI36 |
| NG_008231.1:g.5719G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645694.3:c.471G>A MANE Select | ENSP00000494686.1:p.Leu157= | |
| ENST00000247182.6:c.471G>A | ENSP00000247182.5:p.Leu157= | |
| ENST00000553535.2:n.249-2142G>A | ||
| ENST00000554986.2:c.42-2142G>A | ENSP00000452700.2:n.42-2142G>A | |
| ENST00000555955.3:n.1198-2142G>A | ||
| NM_005982.3:c.471G>A | NP_005973.1:p.Leu157= | |
| XM_017021602.2:c.471G>A | XP_016877091.1:p.Leu157= | |
| NM_005982.4:c.471G>A MANE Select | NP_005973.1:p.Leu157= |