Canonical Allele Identifier: CA2695114883
Gene: EMD HGNC NCBI

Linked Data

gnomAD v4: X-154379293-G-A
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Genomic Alleles

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

Transcript Alleles

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