Canonical Allele Identifier: CA2466663616
Gene: EMD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379293G= , CM000685.2:g.154379293G= GRCh38
NC_000023.10:g.153607653G= , CM000685.1:g.153607653G= GRCh37
NC_000023.9:g.153260847G= NCBI36
NG_008677.1:g.9858G= , LRG_745:g.9858G=
NG_011506.1:g.354C=
NG_011506.2:g.346C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369835.3:c.-192G= ENSP00000358850.3:n.-192G=
ENST00000369842.8:c.-192G= ENSP00000358857.4:n.-192G=
NM_000117.2:c.-192G= , LRG_745t1:c.-192G= NP_000108.1:n.-192G=
XM_024452349.1:c.-400G= XP_024308117.1:n.-400G=
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