Canonical Allele Identifier: CA767343369
Gene: EMILIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1448173635
MyVariant Identifiers: chr2:g.27307614T>C (hg19) chr2:g.27084746T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27084746T>C , CM000664.2:g.27084746T>C GRCh38
NC_000002.11:g.27307614T>C , CM000664.1:g.27307614T>C GRCh37
NC_000002.10:g.27161118T>C NCBI36
NG_012199.1:g.3004T>C
NG_046849.1:g.11180T>C
NG_012199.2:g.3004T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380320.9:c.2557+215T>C MANE Select ENSP00000369677.4:n.2557+215T>C
ENST00000380320.8:c.2557+215T>C ENSP00000369677.4:n.2557+215T>C
ENST00000433140.1:c.549+215T>C
NM_007046.3:c.2557+215T>C NP_008977.1:n.2557+215T>C
XM_006711928.2:c.2557+215T>C XP_006711991.1:n.2557+215T>C
NM_007046.4:c.2557+215T>C MANE Select NP_008977.1:n.2557+215T>C
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