Canonical Allele Identifier: CA337288600

Gene: EMD

Linked Data

• dbSNP Id: rs1046597758
• gnomAD v4: X-154379293-G-T
• MyVariant Identifiers: chrX:g.154379293G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379293G>T , CM000685.2:g.154379293G>T	GRCh38
NC_000023.10:g.153607653G>T , CM000685.1:g.153607653G>T	GRCh37
NC_000023.9:g.153260847G>T	NCBI36
NG_008677.1:g.9858G>T , LRG_745:g.9858G>T
NG_011506.1:g.354C>A
NG_011506.2:g.346C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369835.3:c.-192G>T	ENSP00000358850.3:n.-192G>T
ENST00000369842.8:c.-192G>T	ENSP00000358857.4:n.-192G>T
NM_000117.2:c.-192G>T , LRG_745t1:c.-192G>T	NP_000108.1:n.-192G>T
XM_024452349.1:c.-400G>T	XP_024308117.1:n.-400G>T