Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52224356T>G , CM000665.2:g.52224356T>G | GRCh38 |
| NC_000003.11:g.52258372T>G , CM000665.1:g.52258372T>G | GRCh37 |
| NC_000003.10:g.52233412T>G | NCBI36 |
| NG_033933.1:g.6808A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360658.3:c.4-44A>C MANE Select | ENSP00000353874.2:n.4-44A>C | |
| ENST00000360658.2:c.4-44A>C | ENSP00000353874.2:n.4-44A>C | |
| ENST00000478201.1:c.223-89A>C | ||
| ENST00000494383.1:c.464-44A>C | ||
| NM_017442.3:c.4-44A>C | NP_059138.1:n.4-44A>C | |
| NM_017442.4:c.4-44A>C MANE Select | NP_059138.1:n.4-44A>C |