Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128318219G>A , CM000667.2:g.128318219G>A | GRCh38 |
| NC_000005.9:g.127653911G>A , CM000667.1:g.127653911G>A | GRCh37 |
| NC_000005.8:g.127681810G>A | NCBI36 |
| NG_008750.1:g.224825C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.1431C>T | ||
| ENST00000703785.1:n.1512C>T | ||
| ENST00000262464.9:c.4647C>T MANE Select | ENSP00000262464.4:p.Asn1549= | |
| ENST00000262464.8:c.4647C>T | ENSP00000262464.4:p.Asn1549= | |
| ENST00000508053.5:c.4647C>T | ENSP00000424571.1:p.Asn1549= | |
| ENST00000619499.4:c.4644C>T | ENSP00000482132.1:p.Asn1548= | |
| NM_001999.3:c.4647C>T | NP_001990.2:p.Asn1549= | |
| XM_017009228.2:c.4494C>T | XP_016864717.1:p.Asn1498= | |
| NM_001999.4:c.4647C>T MANE Select | NP_001990.2:p.Asn1549= |