Canonical Allele Identifier: CA337288625
Gene: EMD HGNC NCBI

Linked Data

dbSNP Id: rs1047248195
gnomAD v3: X-154379316-T-A
gnomAD v4: X-154379316-T-A
MyVariant Identifiers: chrX:g.154379316T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379316T>A , CM000685.2:g.154379316T>A GRCh38
NC_000023.10:g.153607676T>A , CM000685.1:g.153607676T>A GRCh37
NC_000023.9:g.153260870T>A NCBI36
NG_008677.1:g.9881T>A , LRG_745:g.9881T>A
NG_011506.1:g.331A>T
NG_011506.2:g.323A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.9:c.-169T>A MANE Select ENSP00000358857.4:n.-169T>A
ENST00000369835.3:c.-169T>A ENSP00000358850.3:n.-169T>A
ENST00000369842.8:c.-169T>A ENSP00000358857.4:n.-169T>A
NM_000117.2:c.-169T>A , LRG_745t1:c.-169T>A NP_000108.1:n.-169T>A
XM_024452349.1:c.-377T>A XP_024308117.1:n.-377T>A
NM_000117.3:c.-169T>A MANE Select NP_000108.1:n.-169T>A
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