Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128301400C>G , CM000667.2:g.128301400C>G | GRCh38 |
| NC_000005.9:g.127637092C>G , CM000667.1:g.127637092C>G | GRCh37 |
| NC_000005.8:g.127664991C>G | NCBI36 |
| NG_008750.1:g.241644G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001999.4:c.6028G>C MANE Select | NP_001990.2:p.Asp2010His |
| ENST00000262464.9:c.6028G>C MANE Select | ENSP00000262464.4:p.Asp2010His |
| NM_001999.3:c.6028G>C | NP_001990.2:p.Asp2010His |
| ENST00000262464.8:c.6028G>C | ENSP00000262464.4:p.Asp2010His |
| ENST00000508053.5:c.6028G>C | ENSP00000424571.1:p.Asp2010His |
| ENST00000619499.4:c.6025G>C | ENSP00000482132.1:p.Asp2009His |
| ENST00000703783.1:n.2812G>C | |
| ENST00000703785.1:n.2731G>C | |
| XM_017009228.2:c.5875G>C | XP_016864717.1:p.Asp1959His |