Canonical Allele Identifier: CA2695114813

Gene: EMD

Linked Data

• gnomAD v4: X-154379218-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379218A>C , CM000685.2:g.154379218A>C	GRCh38
NC_000023.10:g.153607578A>C , CM000685.1:g.153607578A>C	GRCh37
NC_000023.9:g.153260772A>C	NCBI36
NG_008677.1:g.9783A>C , LRG_745:g.9783A>C
NG_011506.1:g.429T>G
NG_011506.2:g.421T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369842.8:c.-267A>C	ENSP00000358857.4:n.-267A>C