Canonical Allele Identifier: CA2695114829
Gene: EMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379234G>A , CM000685.2:g.154379234G>A GRCh38
NC_000023.10:g.153607594G>A , CM000685.1:g.153607594G>A GRCh37
NC_000023.9:g.153260788G>A NCBI36
NG_008677.1:g.9799G>A , LRG_745:g.9799G>A
NG_011506.1:g.413C>T
NG_011506.2:g.405C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.8:c.-251G>A ENSP00000358857.4:n.-251G>A