Canonical Allele Identifier: CA344486398

Gene: IL19

Linked Data

• gnomAD v4: 1-206842617-G-A
• MyVariant Identifiers: chr1:g.207015962G>A (hg19) ; chr1:g.206842617G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206842617G>A , CM000663.2:g.206842617G>A	GRCh38
NC_000001.10:g.207015962G>A , CM000663.1:g.207015962G>A	GRCh37
NC_000001.9:g.205082585G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000659997.3:c.529G>A MANE Select	ENSP00000499459.2:p.Ala177Thr
ENST00000340758.7:c.529G>A	ENSP00000343000.3:p.Ala177Thr
ENST00000656872.2:c.529G>A	ENSP00000499487.2:p.Ala177Thr
ENST00000659997.2:c.529G>A	ENSP00000499459.2:p.Ala177Thr
ENST00000270218.10:c.529G>A	ENSP00000270218.6:p.Ala177Thr
ENST00000340758.6:c.643G>A	ENSP00000343000.2:p.Ala215Thr
ENST00000620365.1:c.529G>A	ENSP00000482668.1:p.Ala177Thr
NM_013371.3:c.529G>A	NP_037503.2:p.Ala177Thr
NM_153758.2:c.643G>A	NP_715639.1:p.Ala215Thr
XR_922482.1:n.205C>T
XR_922482.2:n.205C>T
NM_001369605.1:c.529G>A	NP_001356534.1:p.Ala177Thr
NM_153758.3:c.643G>A	NP_715639.1:p.Ala215Thr
NM_001393490.1:c.529G>A	NP_001380419.1:p.Ala177Thr
NM_001393491.1:c.529G>A	NP_001380420.1:p.Ala177Thr
NM_013371.5:c.529G>A	NP_037503.2:p.Ala177Thr
NM_153758.5:c.529G>A MANE Select	NP_715639.2:p.Ala177Thr