Canonical Allele Identifier: CA2466663568
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379227G= , CM000685.2:g.154379227G= GRCh38
NC_000023.10:g.153607587G= , CM000685.1:g.153607587G= GRCh37
NC_000023.9:g.153260781G= NCBI36
NG_008677.1:g.9792G= , LRG_745:g.9792G=
NG_011506.1:g.420C=
NG_011506.2:g.412C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.8:c.-258G= ENSP00000358857.4:n.-258G=