Canonical Allele Identifier: CA346156379
Gene: EMILIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.27308149T>G (hg19) chr2:g.27085281T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27085281T>G , CM000664.2:g.27085281T>G GRCh38
NC_000002.11:g.27308149T>G , CM000664.1:g.27308149T>G GRCh37
NC_000002.10:g.27161653T>G NCBI36
NG_012199.1:g.3539T>G
NG_046849.1:g.11715T>G
NG_012199.2:g.3539T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380320.9:c.2697T>G MANE Select ENSP00000369677.4:p.Tyr899Ter
ENST00000380320.8:c.2697T>G ENSP00000369677.4:p.Tyr899Ter
ENST00000433140.1:c.689T>G
NM_007046.3:c.2697T>G NP_008977.1:p.Tyr899Ter
XM_006711928.2:c.2575+273T>G XP_006711991.1:n.2575+273T>G
NM_007046.4:c.2697T>G MANE Select NP_008977.1:p.Tyr899Ter
Search 100 bp 5'
Search 100 bp 3'