Canonical Allele Identifier: CA295491240
Gene: EMILIN2 HGNC NCBI

Linked Data

dbSNP Id: rs1008641731
gnomAD v2: 18-2865535-C-T
gnomAD v3: 18-2865537-C-T
gnomAD v4: 18-2865537-C-T
MyVariant Identifiers: chr18:g.2865535C>T (hg19) chr18:g.2865537C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2865537C>T , CM000680.2:g.2865537C>T GRCh38
NC_000018.9:g.2865535C>T , CM000680.1:g.2865535C>T GRCh37
NC_000018.8:g.2855535C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000254528.4:c.257+17606C>T MANE Select ENSP00000254528.3:n.257+17606C>T
ENST00000254528.3:c.257+17606C>T ENSP00000254528.3:n.257+17606C>T
NM_032048.2:c.257+17606C>T NP_114437.2:n.257+17606C>T
XM_011525747.1:c.380+17606C>T XP_011524049.1:n.380+17606C>T
XM_011525748.1:c.380+17606C>T XP_011524050.1:n.380+17606C>T
XR_935070.1:n.699+17606C>T
XM_017026038.2:c.257+17606C>T XP_016881527.1:n.257+17606C>T
NM_032048.3:c.257+17606C>T MANE Select NP_114437.2:n.257+17606C>T
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