Canonical Allele Identifier: CA1240109656

Gene: EMILIN1

Linked Data

• dbSNP Id: rs1558435679

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27085153C>T , CM000664.2:g.27085153C>T	GRCh38
NC_000002.11:g.27308021C>T , CM000664.1:g.27308021C>T	GRCh37
NC_000002.10:g.27161525C>T	NCBI36
NG_012199.1:g.3411C>T
NG_046849.1:g.11587C>T
NG_012199.2:g.3411C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380320.9:c.2576-7C>T MANE Select	ENSP00000369677.4:n.2576-7C>T
ENST00000380320.8:c.2576-7C>T	ENSP00000369677.4:n.2576-7C>T
ENST00000433140.1:c.568-7C>T
NM_007046.3:c.2576-7C>T	NP_008977.1:n.2576-7C>T
XM_006711928.2:c.2575+145C>T	XP_006711991.1:n.2575+145C>T
NM_007046.4:c.2576-7C>T MANE Select	NP_008977.1:n.2576-7C>T