Canonical Allele Identifier: CA873317336

Gene: EMD

Linked Data

• dbSNP Id: rs1226236915
• MyVariant Identifiers: chrX:g.154379355G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379355G>T , CM000685.2:g.154379355G>T	GRCh38
NC_000023.10:g.153607715G>T , CM000685.1:g.153607715G>T	GRCh37
NC_000023.9:g.153260909G>T	NCBI36
NG_008677.1:g.9920G>T , LRG_745:g.9920G>T
NG_011506.1:g.292C>A
NG_011506.2:g.284C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369842.9:c.-130G>T MANE Select	ENSP00000358857.4:n.-130G>T
ENST00000369835.3:c.-130G>T	ENSP00000358850.3:n.-130G>T
ENST00000369842.8:c.-130G>T	ENSP00000358857.4:n.-130G>T
ENST00000486738.5:n.15G>T
NM_000117.2:c.-130G>T , LRG_745t1:c.-130G>T	NP_000108.1:n.-130G>T
XM_024452349.1:c.-338G>T	XP_024308117.1:n.-338G>T
NM_000117.3:c.-130G>T MANE Select	NP_000108.1:n.-130G>T