Canonical Allele Identifier: CA1364116

Gene: IL19

Linked Data

• dbSNP Id: rs370571915
• ExAC: 1:207015959 T / C
• gnomAD v2: 1-207015959-T-C
• gnomAD v3: 1-206842614-T-C
• gnomAD v4: 1-206842614-T-C
• MyVariant Identifiers: chr1:g.207015959T>C (hg19) ; chr1:g.206842614T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206842614T>C , CM000663.2:g.206842614T>C	GRCh38
NC_000001.10:g.207015959T>C , CM000663.1:g.207015959T>C	GRCh37
NC_000001.9:g.205082582T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000659997.3:c.526T>C MANE Select	ENSP00000499459.2:p.Ser176Pro
ENST00000340758.7:c.526T>C	ENSP00000343000.3:p.Ser176Pro
ENST00000656872.2:c.526T>C	ENSP00000499487.2:p.Ser176Pro
ENST00000659997.2:c.526T>C	ENSP00000499459.2:p.Ser176Pro
ENST00000270218.10:c.526T>C	ENSP00000270218.6:p.Ser176Pro
ENST00000340758.6:c.640T>C	ENSP00000343000.2:p.Ser214Pro
ENST00000620365.1:c.526T>C	ENSP00000482668.1:p.Ser176Pro
NM_013371.3:c.526T>C	NP_037503.2:p.Ser176Pro
NM_153758.2:c.640T>C	NP_715639.1:p.Ser214Pro
XR_922482.1:n.208A>G
XR_922482.2:n.208A>G
NM_001369605.1:c.526T>C	NP_001356534.1:p.Ser176Pro
NM_153758.3:c.640T>C	NP_715639.1:p.Ser214Pro
NM_001393490.1:c.526T>C	NP_001380419.1:p.Ser176Pro
NM_001393491.1:c.526T>C	NP_001380420.1:p.Ser176Pro
NM_013371.5:c.526T>C	NP_037503.2:p.Ser176Pro
NM_153758.5:c.526T>C MANE Select	NP_715639.2:p.Ser176Pro