Canonical Allele Identifier: CA279798552
Gene: IL27 HGNC NCBI

Linked Data

dbSNP Id: rs989568768
MyVariant Identifiers: chr16:g.28517612C>T (hg19) chr16:g.28506291C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28506291C>T , CM000678.2:g.28506291C>T GRCh38
NC_000016.9:g.28517612C>T , CM000678.1:g.28517612C>T GRCh37
NC_000016.8:g.28425113C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356897.1:c.31+490G>A MANE Select ENSP00000349365.1:n.31+490G>A
ENST00000568075.1:c.-362-2241G>A ENSP00000455990.1:n.-362-2241G>A
NM_145659.3:c.31+490G>A MANE Select NP_663634.2:n.31+490G>A
XM_011545780.1:c.38-2241G>A XP_011544082.1:n.38-2241G>A
XM_011545780.2:c.38-2241G>A XP_011544082.1:n.38-2241G>A
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