Canonical Allele Identifier: CA873317210
Gene: EMD HGNC NCBI

Linked Data

dbSNP Id: rs1236199059
gnomAD v4: X-154379232-C-T
MyVariant Identifiers: chrX:g.154379232C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379232C>T , CM000685.2:g.154379232C>T GRCh38
NC_000023.10:g.153607592C>T , CM000685.1:g.153607592C>T GRCh37
NC_000023.9:g.153260786C>T NCBI36
NG_008677.1:g.9797C>T , LRG_745:g.9797C>T
NG_011506.1:g.415G>A
NG_011506.2:g.407G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.8:c.-253C>T ENSP00000358857.4:n.-253C>T
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