Canonical Allele Identifier: CA528577745

Gene: IL19

Linked Data

• dbSNP Id: rs1426467755
• gnomAD v2: 1-207015968-T-C
• gnomAD v3: 1-206842623-T-C
• gnomAD v4: 1-206842623-T-C
• MyVariant Identifiers: chr1:g.207015968T>C (hg19) ; chr1:g.206842623T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206842623T>C , CM000663.2:g.206842623T>C	GRCh38
NC_000001.10:g.207015968T>C , CM000663.1:g.207015968T>C	GRCh37
NC_000001.9:g.205082591T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000659997.3:c.*1T>C MANE Select	ENSP00000499459.2:n.*1T>C
ENST00000340758.7:c.*1T>C	ENSP00000343000.3:n.*1T>C
ENST00000656872.2:c.*1T>C	ENSP00000499487.2:n.*1T>C
ENST00000659997.2:c.*1T>C	ENSP00000499459.2:n.*1T>C
ENST00000340758.6:c.*1T>C	ENSP00000343000.2:n.*1T>C
ENST00000620365.1:c.*1T>C	ENSP00000482668.1:n.*1T>C
NM_013371.3:c.*1T>C	NP_037503.2:n.*1T>C
NM_153758.2:c.*1T>C	NP_715639.1:n.*1T>C
XR_922482.1:n.199A>G
XR_922482.2:n.199A>G
NM_001369605.1:c.*1T>C	NP_001356534.1:n.*1T>C
NM_153758.3:c.*1T>C	NP_715639.1:n.*1T>C
NM_001393490.1:c.*1T>C	NP_001380419.1:n.*1T>C
NM_001393491.1:c.*1T>C	NP_001380420.1:n.*1T>C
NM_013371.5:c.*1T>C	NP_037503.2:n.*1T>C
NM_153758.5:c.*1T>C MANE Select	NP_715639.2:n.*1T>C