Canonical Allele Identifier: CA2695114806
Gene: EMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379217del , CM000685.2:g.154379217del GRCh38
NC_000023.10:g.153607577del , CM000685.1:g.153607577del GRCh37
NC_000023.9:g.153260771del NCBI36
NG_008677.1:g.9782del , LRG_745:g.9782del
NG_011506.1:g.433del
NG_011506.2:g.425del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.8:c.-268del ENSP00000358857.4:n.-268del