Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7527122A= , CM000681.2:g.7527122A= | GRCh38 |
| NC_000019.9:g.7592008A= , CM000681.1:g.7592008A= | GRCh37 |
| NC_000019.8:g.7498008A= | NCBI36 |
| NG_015806.1:g.9513A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.571+196A= MANE Select | ENSP00000264079.5:n.571+196A= | |
| ENST00000264079.10:c.571+196A= | ENSP00000264079.5:n.571+196A= | |
| ENST00000394321.9:n.651+196A= | ||
| ENST00000596008.1:n.729A= | ||
| ENST00000598406.1:n.392+196A= | ||
| ENST00000601003.1:c.571+196A= | ENSP00000469074.1:n.571+196A= | |
| NM_020533.2:c.571+196A= | NP_065394.1:n.571+196A= | |
| NM_020533.3:c.571+196A= MANE Select | NP_065394.1:n.571+196A= |