Canonical Allele Identifier: CA344486393

Gene: IL19

Linked Data

• gnomAD v4: 1-206842615-C-T
• COSMIC: COSM4837927 ; COSM4837928
• MyVariant Identifiers: chr1:g.207015960C>T (hg19) ; chr1:g.206842615C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206842615C>T , CM000663.2:g.206842615C>T	GRCh38
NC_000001.10:g.207015960C>T , CM000663.1:g.207015960C>T	GRCh37
NC_000001.9:g.205082583C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659997.3:c.527C>T MANE Select	ENSP00000499459.2:p.Ser176Leu
ENST00000340758.7:c.527C>T	ENSP00000343000.3:p.Ser176Leu
ENST00000656872.2:c.527C>T	ENSP00000499487.2:p.Ser176Leu
ENST00000659997.2:c.527C>T	ENSP00000499459.2:p.Ser176Leu
ENST00000270218.10:c.527C>T	ENSP00000270218.6:p.Ser176Leu
ENST00000340758.6:c.641C>T	ENSP00000343000.2:p.Ser214Leu
ENST00000620365.1:c.527C>T	ENSP00000482668.1:p.Ser176Leu
NM_013371.3:c.527C>T	NP_037503.2:p.Ser176Leu
NM_153758.2:c.641C>T	NP_715639.1:p.Ser214Leu
XR_922482.1:n.207G>A
XR_922482.2:n.207G>A
NM_001369605.1:c.527C>T	NP_001356534.1:p.Ser176Leu
NM_153758.3:c.641C>T	NP_715639.1:p.Ser214Leu
NM_001393490.1:c.527C>T	NP_001380419.1:p.Ser176Leu
NM_001393491.1:c.527C>T	NP_001380420.1:p.Ser176Leu
NM_013371.5:c.527C>T	NP_037503.2:p.Ser176Leu
NM_153758.5:c.527C>T MANE Select	NP_715639.2:p.Ser176Leu