Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6718436A>G , CM000681.2:g.6718436A>G | GRCh38 |
| NC_000019.9:g.6718447A>G , CM000681.1:g.6718447A>G | GRCh37 |
| NC_000019.8:g.6669447A>G | NCBI36 |
| NG_009557.1:g.7216T>C , LRG_27:g.7216T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000594936.2:n.329-24T>C | ||
| ENST00000695652.1:c.145-24T>C | ENSP00000512083.1:n.145-24T>C | |
| ENST00000695693.1:c.268-24T>C | ENSP00000512104.1:n.268-24T>C | |
| ENST00000245907.11:c.268-24T>C MANE Select | ENSP00000245907.4:n.268-24T>C | |
| ENST00000245907.10:c.268-24T>C | ENSP00000245907.4:n.268-24T>C | |
| ENST00000594936.1:n.329-24T>C | ||
| ENST00000600744.1:c.145-24T>C | ENSP00000472044.1:n.145-24T>C | |
| NM_000064.3:c.268-24T>C | NP_000055.2:n.268-24T>C | |
| NM_000064.4:c.268-24T>C MANE Select | NP_000055.2:n.268-24T>C |