Canonical Allele Identifier: CA2695114869
Gene: EMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379270A>C , CM000685.2:g.154379270A>C GRCh38
NC_000023.10:g.153607630A>C , CM000685.1:g.153607630A>C GRCh37
NC_000023.9:g.153260824A>C NCBI36
NG_008677.1:g.9835A>C , LRG_745:g.9835A>C
NG_011506.1:g.377T>G
NG_011506.2:g.369T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.8:c.-215A>C ENSP00000358857.4:n.-215A>C
NM_000117.2:c.-215A>C , LRG_745t1:c.-215A>C NP_000108.1:n.-215A>C
XM_024452349.1:c.-423A>C XP_024308117.1:n.-423A>C