Canonical Allele Identifier: CA346156323
Gene: EMILIN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.27308133T>G (hg19) chr2:g.27085265T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27085265T>G , CM000664.2:g.27085265T>G GRCh38
NC_000002.11:g.27308133T>G , CM000664.1:g.27308133T>G GRCh37
NC_000002.10:g.27161637T>G NCBI36
NG_012199.1:g.3523T>G
NG_046849.1:g.11699T>G
NG_012199.2:g.3523T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380320.9:c.2681T>G MANE Select ENSP00000369677.4:p.Leu894Arg
ENST00000380320.8:c.2681T>G ENSP00000369677.4:p.Leu894Arg
ENST00000433140.1:c.673T>G
NM_007046.3:c.2681T>G NP_008977.1:p.Leu894Arg
XM_006711928.2:c.2575+257T>G XP_006711991.1:n.2575+257T>G
NM_007046.4:c.2681T>G MANE Select NP_008977.1:p.Leu894Arg
Search 100 bp 5'
Search 100 bp 3'