Canonical Allele Identifier: CA344486409

Gene: IL19

Linked Data

• gnomAD v4: 1-206842621-G-T
• MyVariant Identifiers: chr1:g.207015966G>T (hg19) ; chr1:g.206842621G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206842621G>T , CM000663.2:g.206842621G>T	GRCh38
NC_000001.10:g.207015966G>T , CM000663.1:g.207015966G>T	GRCh37
NC_000001.9:g.205082589G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659997.3:c.533G>T MANE Select	ENSP00000499459.2:p.Ter178Leu
ENST00000340758.7:c.533G>T	ENSP00000343000.3:p.Ter178Leu
ENST00000656872.2:c.533G>T	ENSP00000499487.2:p.Ter178Leu
ENST00000659997.2:c.533G>T	ENSP00000499459.2:p.Ter178Leu
ENST00000270218.10:c.533G>T	ENSP00000270218.6:p.Ter178Leu
ENST00000340758.6:c.647G>T	ENSP00000343000.2:p.Ter216Leu
ENST00000620365.1:c.533G>T	ENSP00000482668.1:p.Ter178Leu
NM_013371.3:c.533G>T	NP_037503.2:p.Ter178Leu
NM_153758.2:c.647G>T	NP_715639.1:p.Ter216Leu
XR_922482.1:n.201C>A
XR_922482.2:n.201C>A
NM_001369605.1:c.533G>T	NP_001356534.1:p.Ter178Leu
NM_153758.3:c.647G>T	NP_715639.1:p.Ter216Leu
NM_001393490.1:c.533G>T	NP_001380419.1:p.Ter178Leu
NM_001393491.1:c.533G>T	NP_001380420.1:p.Ter178Leu
NM_013371.5:c.533G>T	NP_037503.2:p.Ter178Leu
NM_153758.5:c.533G>T MANE Select	NP_715639.2:p.Ter178Leu