Canonical Allele Identifier: CA2650221029

Gene: IL19

Linked Data

• gnomAD v4: 1-206842624-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206842624G>A , CM000663.2:g.206842624G>A	GRCh38
NC_000001.10:g.207015969G>A , CM000663.1:g.207015969G>A	GRCh37
NC_000001.9:g.205082592G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659997.3:c.*2G>A MANE Select	ENSP00000499459.2:n.*2G>A
ENST00000340758.7:c.*2G>A	ENSP00000343000.3:n.*2G>A
ENST00000656872.2:c.*2G>A	ENSP00000499487.2:n.*2G>A
ENST00000659997.2:c.*2G>A	ENSP00000499459.2:n.*2G>A
ENST00000340758.6:c.*2G>A	ENSP00000343000.2:n.*2G>A
ENST00000620365.1:c.*2G>A	ENSP00000482668.1:n.*2G>A
NM_013371.3:c.*2G>A	NP_037503.2:n.*2G>A
NM_153758.2:c.*2G>A	NP_715639.1:n.*2G>A
XR_922482.1:n.198C>T
XR_922482.2:n.198C>T
NM_001369605.1:c.*2G>A	NP_001356534.1:n.*2G>A
NM_153758.3:c.*2G>A	NP_715639.1:n.*2G>A
NM_001393490.1:c.*2G>A	NP_001380419.1:n.*2G>A
NM_001393491.1:c.*2G>A	NP_001380420.1:n.*2G>A
NM_013371.5:c.*2G>A	NP_037503.2:n.*2G>A
NM_153758.5:c.*2G>A MANE Select	NP_715639.2:n.*2G>A