Canonical Allele Identifier: CA337288533
Gene: EMD HGNC NCBI

Linked Data

dbSNP Id: rs954667554
MyVariant Identifiers: chrX:g.154379226A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379226A>T , CM000685.2:g.154379226A>T GRCh38
NC_000023.10:g.153607586A>T , CM000685.1:g.153607586A>T GRCh37
NC_000023.9:g.153260780A>T NCBI36
NG_008677.1:g.9791A>T , LRG_745:g.9791A>T
NG_011506.1:g.421T>A
NG_011506.2:g.413T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.8:c.-259A>T ENSP00000358857.4:n.-259A>T
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