Canonical Allele Identifier: CA2695114825
Gene: EMD HGNC NCBI

Linked Data

gnomAD v4: X-154379228-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379228C>A , CM000685.2:g.154379228C>A GRCh38
NC_000023.10:g.153607588C>A , CM000685.1:g.153607588C>A GRCh37
NC_000023.9:g.153260782C>A NCBI36
NG_008677.1:g.9793C>A , LRG_745:g.9793C>A
NG_011506.1:g.419G>T
NG_011506.2:g.411G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.8:c.-257C>A ENSP00000358857.4:n.-257C>A
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