Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6718442C>T , CM000681.2:g.6718442C>T | GRCh38 |
| NC_000019.9:g.6718453C>T , CM000681.1:g.6718453C>T | GRCh37 |
| NC_000019.8:g.6669453C>T | NCBI36 |
| NG_009557.1:g.7210G>A , LRG_27:g.7210G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000594936.2:n.329-30G>A | ||
| ENST00000695652.1:c.145-30G>A | ENSP00000512083.1:n.145-30G>A | |
| ENST00000695693.1:c.268-30G>A | ENSP00000512104.1:n.268-30G>A | |
| ENST00000245907.11:c.268-30G>A MANE Select | ENSP00000245907.4:n.268-30G>A | |
| ENST00000245907.10:c.268-30G>A | ENSP00000245907.4:n.268-30G>A | |
| ENST00000594936.1:n.329-30G>A | ||
| ENST00000600744.1:c.145-30G>A | ENSP00000472044.1:n.145-30G>A | |
| NM_000064.3:c.268-30G>A | NP_000055.2:n.268-30G>A | |
| NM_000064.4:c.268-30G>A MANE Select | NP_000055.2:n.268-30G>A |