Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159327201C>A , CM000667.2:g.159327201C>A | GRCh38 |
| NC_000005.9:g.158754209C>A , CM000667.1:g.158754209C>A | GRCh37 |
| NC_000005.8:g.158686787C>A | NCBI36 |
| NG_009618.1:g.8273G>T , LRG_71:g.8273G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696750.1:c.-149+3231G>T | ENSP00000512849.1:n.-149+3231G>T | |
| ENST00000696751.1:c.1-419G>T | ENSP00000512850.1:n.1-419G>T | |
| ENST00000696752.1:n.433-419G>T | ||
| ENST00000231228.3:c.1-419G>T MANE Select | ENSP00000231228.2:n.1-419G>T | |
| ENST00000231228.2:c.1-419G>T | ENSP00000231228.2:n.1-419G>T | |
| NM_002187.2:c.1-419G>T , LRG_71t1:c.1-419G>T | NP_002178.2:n.1-419G>T | |
| NM_002187.3:c.1-419G>T MANE Select | NP_002178.2:n.1-419G>T |