Canonical Allele Identifier: CA873317360
Gene: EMD HGNC NCBI

Linked Data

dbSNP Id: rs1167211453
MyVariant Identifiers: chrX:g.154379409T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379409T>C , CM000685.2:g.154379409T>C GRCh38
NC_000023.10:g.153607769T>C , CM000685.1:g.153607769T>C GRCh37
NC_000023.9:g.153260963T>C NCBI36
NG_008677.1:g.9974T>C , LRG_745:g.9974T>C
NG_011506.1:g.238A>G
NG_011506.2:g.230A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.9:c.-76T>C MANE Select ENSP00000358857.4:n.-76T>C
ENST00000369835.3:c.-76T>C ENSP00000358850.3:n.-76T>C
ENST00000369842.8:c.-76T>C ENSP00000358857.4:n.-76T>C
ENST00000428228.5:c.-76T>C ENSP00000401081.1:n.-76T>C
ENST00000485261.1:n.6T>C
ENST00000486738.5:n.69T>C
NM_000117.2:c.-76T>C , LRG_745t1:c.-76T>C NP_000108.1:n.-76T>C
XM_024452349.1:c.-284T>C XP_024308117.1:n.-284T>C
NM_000117.3:c.-76T>C MANE Select NP_000108.1:n.-76T>C
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