Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135031850A>G , CM000667.2:g.135031850A>G | GRCh38 |
| NC_000005.9:g.134367540A>G , CM000667.1:g.134367540A>G | GRCh37 |
| NC_000005.8:g.134395439A>G | NCBI36 |
| NG_012114.1:g.7425T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002653.5:c.170-342T>C MANE Select | NP_002644.4:n.170-342T>C |
| ENST00000265340.12:c.170-342T>C MANE Select | ENSP00000265340.6:n.170-342T>C |
| NM_002653.4:c.170-342T>C | NP_002644.4:n.170-342T>C |
| ENST00000265340.11:c.170-342T>C | ENSP00000265340.6:n.170-342T>C |
| ENST00000502676.1:c.170-342T>C | ENSP00000423624.1:n.170-342T>C |
| ENST00000503586.1:c.292-342T>C | |
| ENST00000504936.1:n.161T>C | |
| ENST00000506438.5:c.170-342T>C | ENSP00000427542.1:n.170-342T>C |
| ENST00000507253.5:c.170-342T>C | ENSP00000422908.1:n.170-342T>C |