Canonical Allele Identifier: CA422935085

Gene: IL19

Linked Data

• MyVariant Identifiers: chr1:g.207015961A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206842616A>C , CM000663.2:g.206842616A>C	GRCh38
NC_000001.10:g.207015961A>C , CM000663.1:g.207015961A>C	GRCh37
NC_000001.9:g.205082584A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659997.3:c.528A>C MANE Select	ENSP00000499459.2:p.Ser176=
ENST00000340758.7:c.528A>C	ENSP00000343000.3:p.Ser176=
ENST00000656872.2:c.528A>C	ENSP00000499487.2:p.Ser176=
ENST00000659997.2:c.528A>C	ENSP00000499459.2:p.Ser176=
ENST00000270218.10:c.528A>C	ENSP00000270218.6:p.Ser176=
ENST00000340758.6:c.642A>C	ENSP00000343000.2:p.Ser214=
ENST00000620365.1:c.528A>C	ENSP00000482668.1:p.Ser176=
NM_013371.3:c.528A>C	NP_037503.2:p.Ser176=
NM_153758.2:c.642A>C	NP_715639.1:p.Ser214=
XR_922482.1:n.206T>G
XR_922482.2:n.206T>G
NM_001369605.1:c.528A>C	NP_001356534.1:p.Ser176=
NM_153758.3:c.642A>C	NP_715639.1:p.Ser214=
NM_001393490.1:c.528A>C	NP_001380419.1:p.Ser176=
NM_001393491.1:c.528A>C	NP_001380420.1:p.Ser176=
NM_013371.5:c.528A>C	NP_037503.2:p.Ser176=
NM_153758.5:c.528A>C MANE Select	NP_715639.2:p.Ser176=