Canonical Allele Identifier: CA767343422
Gene: EMILIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1467968534
gnomAD v3: 2-27084833-A-C
gnomAD v4: 2-27084833-A-C
MyVariant Identifiers: chr2:g.27307701A>C (hg19) chr2:g.27084833A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27084833A>C , CM000664.2:g.27084833A>C GRCh38
NC_000002.11:g.27307701A>C , CM000664.1:g.27307701A>C GRCh37
NC_000002.10:g.27161205A>C NCBI36
NG_012199.1:g.3091A>C
NG_046849.1:g.11267A>C
NG_012199.2:g.3091A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000380320.9:c.2558-158A>C MANE Select ENSP00000369677.4:n.2558-158A>C
ENST00000380320.8:c.2558-158A>C ENSP00000369677.4:n.2558-158A>C
ENST00000433140.1:c.550-158A>C
NM_007046.3:c.2558-158A>C NP_008977.1:n.2558-158A>C
XM_006711928.2:c.2558-158A>C XP_006711991.1:n.2558-158A>C
NM_007046.4:c.2558-158A>C MANE Select NP_008977.1:n.2558-158A>C
Search 100 bp 5'
Search 100 bp 3'