Canonical Allele Identifier: CA2658282943
Gene: EMILIN1 HGNC NCBI

Linked Data

gnomAD v4: 2-27084903-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27084903G>T , CM000664.2:g.27084903G>T GRCh38
NC_000002.11:g.27307771G>T , CM000664.1:g.27307771G>T GRCh37
NC_000002.10:g.27161275G>T NCBI36
NG_012199.1:g.3161G>T
NG_046849.1:g.11337G>T
NG_012199.2:g.3161G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380320.9:c.2558-88G>T MANE Select ENSP00000369677.4:n.2558-88G>T
ENST00000380320.8:c.2558-88G>T ENSP00000369677.4:n.2558-88G>T
ENST00000433140.1:c.550-88G>T
NM_007046.3:c.2558-88G>T NP_008977.1:n.2558-88G>T
XM_006711928.2:c.2558-88G>T XP_006711991.1:n.2558-88G>T
NM_007046.4:c.2558-88G>T MANE Select NP_008977.1:n.2558-88G>T