Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21738870A>T , CM000669.2:g.21738870A>T | GRCh38 |
| NC_000007.13:g.21778488A>T , CM000669.1:g.21778488A>T | GRCh37 |
| NC_000007.12:g.21745013A>T | NCBI36 |
| NG_012886.2:g.200656A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.7811+4A>T MANE Select | NP_001264044.1:n.7811+4A>T |
| ENST00000409508.8:c.7811+4A>T MANE Select | ENSP00000475939.1:n.7811+4A>T |
| NM_001277115.1:c.7811+4A>T | NP_001264044.1:n.7811+4A>T |
| ENST00000328843.10:c.7832+4A>T | ENSP00000330671.7:n.7832+4A>T |
| ENST00000409508.7:c.7811+4A>T | ENSP00000475939.1:n.7811+4A>T |
| ENST00000605912.1:c.371+4A>T | ENSP00000476068.1:n.371+4A>T |
| ENST00000620169.4:c.7832+4A>T | ENSP00000481693.1:n.7832+4A>T |