Canonical Allele Identifier: CA337288544
Gene: EMD HGNC NCBI

Linked Data

dbSNP Id: rs782082551

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379227G>C , CM000685.2:g.154379227G>C GRCh38
NC_000023.10:g.153607587G>C , CM000685.1:g.153607587G>C GRCh37
NC_000023.9:g.153260781G>C NCBI36
NG_008677.1:g.9792G>C , LRG_745:g.9792G>C
NG_011506.1:g.420C>G
NG_011506.2:g.412C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.8:c.-258G>C ENSP00000358857.4:n.-258G>C