HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94047242_94047245del , CM000663.2:g.94047242_94047245del | GRCh38 |
NC_000001.10:g.94512798_94512801del , CM000663.1:g.94512798_94512801del | GRCh37 |
NC_000001.9:g.94285386_94285389del | NCBI36 |
NG_009073.1:g.78905_78908del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2744-152_2744-149del MANE Select | ENSP00000359245.3:n.2744-152_2744-149del | |
ENST00000649773.1:c.2522-152_2522-149del | ENSP00000496882.1:n.2522-152_2522-149del | |
ENST00000370225.3:c.2744-152_2744-149del | ENSP00000359245.3:n.2744-152_2744-149del | |
ENST00000536513.5:c.-64-7156_-64-7153del | ENSP00000439707.2:n.-64-7156_-64-7153del | |
NM_000350.2:c.2744-152_2744-149del | NP_000341.2:n.2744-152_2744-149del | |
NM_000350.3:c.2744-152_2744-149del MANE Select | NP_000341.2:n.2744-152_2744-149del |