Canonical Allele Identifier: CA2466663614
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379291G= , CM000685.2:g.154379291G= GRCh38
NC_000023.10:g.153607651G= , CM000685.1:g.153607651G= GRCh37
NC_000023.9:g.153260845G= NCBI36
NG_008677.1:g.9856G= , LRG_745:g.9856G=
NG_011506.1:g.356C=
NG_011506.2:g.348C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369835.3:c.-194G= ENSP00000358850.3:n.-194G=
ENST00000369842.8:c.-194G= ENSP00000358857.4:n.-194G=
NM_000117.2:c.-194G= , LRG_745t1:c.-194G= NP_000108.1:n.-194G=
XM_024452349.1:c.-402G= XP_024308117.1:n.-402G=