Canonical Allele Identifier: CA425382183
Gene: EMILIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.27308071T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27085203T>C , CM000664.2:g.27085203T>C GRCh38
NC_000002.11:g.27308071T>C , CM000664.1:g.27308071T>C GRCh37
NC_000002.10:g.27161575T>C NCBI36
NG_012199.1:g.3461T>C
NG_046849.1:g.11637T>C
NG_012199.2:g.3461T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380320.9:c.2619T>C MANE Select ENSP00000369677.4:p.Phe873=
ENST00000380320.8:c.2619T>C ENSP00000369677.4:p.Phe873=
ENST00000433140.1:c.611T>C
NM_007046.3:c.2619T>C NP_008977.1:p.Phe873=
XM_006711928.2:c.2575+195T>C XP_006711991.1:n.2575+195T>C
NM_007046.4:c.2619T>C MANE Select NP_008977.1:p.Phe873=
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