Canonical Allele Identifier: CA1139923040

Gene: IL19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206841127A= , CM000663.2:g.206841127A=	GRCh38
NC_000001.10:g.207014472A= , CM000663.1:g.207014472A=	GRCh37
NC_000001.9:g.205081095A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_153758.5:c.438+49A= MANE Select	NP_715639.2:n.438+49A=
ENST00000659997.3:c.438+49A= MANE Select	ENSP00000499459.2:n.438+49A=
NM_001369605.1:c.438+49A=	NP_001356534.1:n.438+49A=
NM_001393490.1:c.438+49A=	NP_001380419.1:n.438+49A=
NM_001393491.1:c.438+49A=	NP_001380420.1:n.438+49A=
NM_013371.3:c.438+49A=	NP_037503.2:n.438+49A=
NM_013371.5:c.438+49A=	NP_037503.2:n.438+49A=
NM_153758.2:c.552+49A=	NP_715639.1:n.552+49A=
NM_153758.3:c.552+49A=	NP_715639.1:n.552+49A=
ENST00000270218.10:c.438+49A=	ENSP00000270218.6:n.438+49A=
ENST00000340758.6:c.552+49A=	ENSP00000343000.2:n.552+49A=
ENST00000340758.7:c.438+49A=	ENSP00000343000.3:n.438+49A=
ENST00000620365.1:c.438+49A=	ENSP00000482668.1:n.438+49A=
ENST00000656872.2:c.438+49A=	ENSP00000499487.2:n.438+49A=
ENST00000659997.2:c.438+49A=	ENSP00000499459.2:n.438+49A=
XR_922482.1:n.701T=
XR_922482.2:n.701T=