Linked Data
MyVariant Identifiers:
chr11:g.64518930A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64751458A>T , CM000673.2:g.64751458A>T | GRCh38 |
| NC_000011.9:g.64518930A>T , CM000673.1:g.64518930A>T | GRCh37 |
| NC_000011.8:g.64275506A>T | NCBI36 |
| NG_013018.1:g.14258T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000164139.4:c.1836T>A MANE Select | ENSP00000164139.3:p.Pro612= | |
| ENST00000164139.3:c.1836T>A | ENSP00000164139.3:p.Pro612= | |
| ENST00000377432.7:c.1572T>A | ENSP00000366650.3:p.Pro524= | |
| ENST00000462303.1:n.160T>A | ||
| NM_001164716.1:c.1572T>A | NP_001158188.1:p.Pro524= | |
| NM_005609.2:c.1836T>A | NP_005600.1:p.Pro612= | |
| NM_005609.3:c.1836T>A | NP_005600.1:p.Pro612= | |
| NM_005609.4:c.1836T>A MANE Select | NP_005600.1:p.Pro612= |