Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45804058A>G , CM000681.2:g.45804058A>G | GRCh38 |
| NC_000019.9:g.46307316A>G , CM000681.1:g.46307316A>G | GRCh37 |
| NC_000019.8:g.50999156A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221538.8:c.1653+194T>C MANE Select | ENSP00000221538.2:n.1653+194T>C | |
| ENST00000221538.7:c.1653+194T>C | ENSP00000221538.2:n.1653+194T>C | |
| ENST00000597055.1:c.1653+194T>C | ENSP00000472630.1:n.1653+194T>C | |
| ENST00000600188.5:c.861+194T>C | ENSP00000471559.1:n.861+194T>C | |
| NM_030785.3:c.1653+194T>C | NP_110412.1:n.1653+194T>C | |
| XM_011527351.1:c.1653+194T>C | XP_011525653.1:n.1653+194T>C | |
| XM_011527351.2:c.1653+194T>C | XP_011525653.1:n.1653+194T>C | |
| NM_030785.4:c.1653+194T>C MANE Select | NP_110412.1:n.1653+194T>C |