Canonical Allele Identifier: CA36576321

Gene: IL19

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206802774T>C , CM000663.2:g.206802774T>C	GRCh38
NC_000001.10:g.206976119T>C , CM000663.1:g.206976119T>C	GRCh37
NC_000001.9:g.205042742T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659997.3:c.-3+3768T>C MANE Select	ENSP00000499459.2:n.-3+3768T>C
ENST00000656872.2:c.-3+3768T>C	ENSP00000499487.2:n.-3+3768T>C
ENST00000659997.2:c.-3+3768T>C	ENSP00000499459.2:n.-3+3768T>C
ENST00000662320.1:n.213+3768T>C
ENST00000340758.6:c.112+3768T>C	ENSP00000343000.2:n.112+3768T>C
NM_153758.2:c.112+3768T>C	NP_715639.1:n.112+3768T>C
NM_153758.3:c.112+3768T>C	NP_715639.1:n.112+3768T>C
NM_001393490.1:c.-3+3768T>C	NP_001380419.1:n.-3+3768T>C
NM_153758.5:c.-3+3768T>C MANE Select	NP_715639.2:n.-3+3768T>C