Canonical Allele Identifier: CA10749985

Gene: IL19

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206809585A>T , CM000663.2:g.206809585A>T	GRCh38
NC_000001.10:g.206982930A>T , CM000663.1:g.206982930A>T	GRCh37
NC_000001.9:g.205049553A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659997.3:c.-3+10579A>T MANE Select	ENSP00000499459.2:n.-3+10579A>T
ENST00000656872.2:c.-3+10579A>T	ENSP00000499487.2:n.-3+10579A>T
ENST00000659997.2:c.-3+10579A>T	ENSP00000499459.2:n.-3+10579A>T
ENST00000662320.1:n.213+10579A>T
ENST00000340758.6:c.112+10579A>T	ENSP00000343000.2:n.112+10579A>T
NM_153758.2:c.112+10579A>T	NP_715639.1:n.112+10579A>T
NM_153758.3:c.112+10579A>T	NP_715639.1:n.112+10579A>T
NM_001393490.1:c.-3+10579A>T	NP_001380419.1:n.-3+10579A>T
NM_153758.5:c.-3+10579A>T MANE Select	NP_715639.2:n.-3+10579A>T