Canonical Allele Identifier: CA344486383

Gene: IL19

Linked Data

• gnomAD v4: 1-206842613-C-A
• MyVariant Identifiers: chr1:g.207015958C>A (hg19) ; chr1:g.206842613C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206842613C>A , CM000663.2:g.206842613C>A	GRCh38
NC_000001.10:g.207015958C>A , CM000663.1:g.207015958C>A	GRCh37
NC_000001.9:g.205082581C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659997.3:c.525C>A MANE Select	ENSP00000499459.2:p.Phe175Leu
ENST00000340758.7:c.525C>A	ENSP00000343000.3:p.Phe175Leu
ENST00000656872.2:c.525C>A	ENSP00000499487.2:p.Phe175Leu
ENST00000659997.2:c.525C>A	ENSP00000499459.2:p.Phe175Leu
ENST00000270218.10:c.525C>A	ENSP00000270218.6:p.Phe175Leu
ENST00000340758.6:c.639C>A	ENSP00000343000.2:p.Phe213Leu
ENST00000620365.1:c.525C>A	ENSP00000482668.1:p.Phe175Leu
NM_013371.3:c.525C>A	NP_037503.2:p.Phe175Leu
NM_153758.2:c.639C>A	NP_715639.1:p.Phe213Leu
XR_922482.1:n.209G>T
XR_922482.2:n.209G>T
NM_001369605.1:c.525C>A	NP_001356534.1:p.Phe175Leu
NM_153758.3:c.639C>A	NP_715639.1:p.Phe213Leu
NM_001393490.1:c.525C>A	NP_001380419.1:p.Phe175Leu
NM_001393491.1:c.525C>A	NP_001380420.1:p.Phe175Leu
NM_013371.5:c.525C>A	NP_037503.2:p.Phe175Leu
NM_153758.5:c.525C>A MANE Select	NP_715639.2:p.Phe175Leu