Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135031896A>G , CM000667.2:g.135031896A>G | GRCh38 |
| NC_000005.9:g.134367586A>G , CM000667.1:g.134367586A>G | GRCh37 |
| NC_000005.8:g.134395485A>G | NCBI36 |
| NG_012114.1:g.7379T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.170-388T>C MANE Select | ENSP00000265340.6:n.170-388T>C | |
| ENST00000265340.11:c.170-388T>C | ENSP00000265340.6:n.170-388T>C | |
| ENST00000502676.1:c.170-388T>C | ENSP00000423624.1:n.170-388T>C | |
| ENST00000503586.1:c.292-388T>C | ||
| ENST00000504936.1:n.115T>C | ||
| ENST00000506438.5:c.170-388T>C | ENSP00000427542.1:n.170-388T>C | |
| ENST00000507253.5:c.170-388T>C | ENSP00000422908.1:n.170-388T>C | |
| NM_002653.4:c.170-388T>C | NP_002644.4:n.170-388T>C | |
| NM_002653.5:c.170-388T>C MANE Select | NP_002644.4:n.170-388T>C |