Canonical Allele Identifier: CA873317269

Gene: EMD

Linked Data

• dbSNP Id: rs1324666334
• gnomAD v3: X-154379273-T-A
• gnomAD v4: X-154379273-T-A
• MyVariant Identifiers: chrX:g.154379273T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379273T>A , CM000685.2:g.154379273T>A	GRCh38
NC_000023.10:g.153607633T>A , CM000685.1:g.153607633T>A	GRCh37
NC_000023.9:g.153260827T>A	NCBI36
NG_008677.1:g.9838T>A , LRG_745:g.9838T>A
NG_011506.1:g.374A>T
NG_011506.2:g.366A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369835.3:c.-212T>A	ENSP00000358850.3:n.-212T>A
ENST00000369842.8:c.-212T>A	ENSP00000358857.4:n.-212T>A
NM_000117.2:c.-212T>A , LRG_745t1:c.-212T>A	NP_000108.1:n.-212T>A
XM_024452349.1:c.-420T>A	XP_024308117.1:n.-420T>A