Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50150188A>T , CM000676.2:g.50150188A>T | GRCh38 |
| NC_000014.8:g.50616906A>T , CM000676.1:g.50616906A>T | GRCh37 |
| NC_000014.7:g.49686656A>T | NCBI36 |
| NG_051073.1:g.86506T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216373.10:c.2204T>A MANE Select | ENSP00000216373.5:p.Ile735Asn | |
| ENST00000216373.9:c.2204T>A | ENSP00000216373.5:p.Ile735Asn | |
| ENST00000543680.5:c.2105T>A | ENSP00000445328.1:p.Ile702Asn | |
| NM_006939.2:c.2204T>A | NP_008870.2:p.Ile735Asn | |
| XM_005268021.1:c.2024T>A | XP_005268078.1:p.Ile675Asn | |
| XM_011537103.1:c.2165T>A | XP_011535405.1:p.Ile722Asn | |
| XM_011537104.1:c.2204T>A | XP_011535406.1:p.Ile735Asn | |
| NM_006939.3:c.2204T>A | NP_008870.2:p.Ile735Asn | |
| NM_006939.4:c.2204T>A MANE Select | NP_008870.2:p.Ile735Asn |