Canonical Allele Identifier: CA778147738
Gene: EMILIN2 HGNC NCBI

Linked Data

dbSNP Id: rs755921629
MyVariant Identifiers: chr18:g.2865529G>A (hg19) chr18:g.2865531G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2865531G>A , CM000680.2:g.2865531G>A GRCh38
NC_000018.9:g.2865529G>A , CM000680.1:g.2865529G>A GRCh37
NC_000018.8:g.2855529G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000254528.4:c.257+17600G>A MANE Select ENSP00000254528.3:n.257+17600G>A
ENST00000254528.3:c.257+17600G>A ENSP00000254528.3:n.257+17600G>A
NM_032048.2:c.257+17600G>A NP_114437.2:n.257+17600G>A
XM_011525747.1:c.380+17600G>A XP_011524049.1:n.380+17600G>A
XM_011525748.1:c.380+17600G>A XP_011524050.1:n.380+17600G>A
XR_935070.1:n.699+17600G>A
XM_017026038.2:c.257+17600G>A XP_016881527.1:n.257+17600G>A
NM_032048.3:c.257+17600G>A MANE Select NP_114437.2:n.257+17600G>A
Search 100 bp 5'
Search 100 bp 3'