Canonical Allele Identifier: CA2658282760
Gene: EMILIN1 HGNC NCBI

Linked Data

gnomAD v4: 2-27084861-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27084861C>T , CM000664.2:g.27084861C>T GRCh38
NC_000002.11:g.27307729C>T , CM000664.1:g.27307729C>T GRCh37
NC_000002.10:g.27161233C>T NCBI36
NG_012199.1:g.3119C>T
NG_046849.1:g.11295C>T
NG_012199.2:g.3119C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380320.9:c.2558-130C>T MANE Select ENSP00000369677.4:n.2558-130C>T
ENST00000380320.8:c.2558-130C>T ENSP00000369677.4:n.2558-130C>T
ENST00000433140.1:c.550-130C>T
NM_007046.3:c.2558-130C>T NP_008977.1:n.2558-130C>T
XM_006711928.2:c.2558-130C>T XP_006711991.1:n.2558-130C>T
NM_007046.4:c.2558-130C>T MANE Select NP_008977.1:n.2558-130C>T
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