Canonical Allele Identifier: CA425382291
Gene: EMILIN1 HGNC NCBI

Linked Data

gnomAD v4: 2-27085290-A-G
MyVariant Identifiers: chr2:g.27308158A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27085290A>G , CM000664.2:g.27085290A>G GRCh38
NC_000002.11:g.27308158A>G , CM000664.1:g.27308158A>G GRCh37
NC_000002.10:g.27161662A>G NCBI36
NG_012199.1:g.3548A>G
NG_046849.1:g.11724A>G
NG_012199.2:g.3548A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380320.9:c.2706A>G MANE Select ENSP00000369677.4:p.Pro902=
ENST00000380320.8:c.2706A>G ENSP00000369677.4:p.Pro902=
ENST00000433140.1:c.698A>G
NM_007046.3:c.2706A>G NP_008977.1:p.Pro902=
XM_006711928.2:c.2575+282A>G XP_006711991.1:n.2575+282A>G
NM_007046.4:c.2706A>G MANE Select NP_008977.1:p.Pro902=
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