Canonical Allele Identifier: CA2695114881
Gene: EMD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379290C>A , CM000685.2:g.154379290C>A GRCh38
NC_000023.10:g.153607650C>A , CM000685.1:g.153607650C>A GRCh37
NC_000023.9:g.153260844C>A NCBI36
NG_008677.1:g.9855C>A , LRG_745:g.9855C>A
NG_011506.1:g.357G>T
NG_011506.2:g.349G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369835.3:c.-195C>A ENSP00000358850.3:n.-195C>A
ENST00000369842.8:c.-195C>A ENSP00000358857.4:n.-195C>A
NM_000117.2:c.-195C>A , LRG_745t1:c.-195C>A NP_000108.1:n.-195C>A
XM_024452349.1:c.-403C>A XP_024308117.1:n.-403C>A