Canonical Allele Identifier: CA2466663562
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379214C= , CM000685.2:g.154379214C= GRCh38
NC_000023.10:g.153607574C= , CM000685.1:g.153607574C= GRCh37
NC_000023.9:g.153260768C= NCBI36
NG_008677.1:g.9779C= , LRG_745:g.9779C=
NG_011506.1:g.433G=
NG_011506.2:g.425G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.8:c.-271C= ENSP00000358857.4:n.-271C=