Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190388019T= , CM000665.2:g.190388019T= | GRCh38 |
| NC_000003.11:g.190105808T= , CM000665.1:g.190105808T= | GRCh37 |
| NC_000003.10:g.191588502T= | NCBI36 |
| NG_008149.1:g.4968T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.2:c.-101T= | ENSP00000264734.2:n.-101T= | |
| ENST00000468220.1:n.306+13416T= | ||
| NM_006580.3:c.-101T= | NP_006571.1:n.-101T= | |
| NM_001378492.1:c.-93-218T= | NP_001365421.1:n.-93-218T= | |
| NM_001378493.1:c.-93-218T= | NP_001365422.1:n.-93-218T= |