Canonical Allele Identifier: CA10575499
Gene: CHI3L1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.203186754G>C
GRCh37 chr1:g.203155882G>C
gnomAD v2:
1:203155882 G / C
gnomAD v3:
1:203186754 G / C
gnomAD v4:
chr1-203186754-G-C
Joint Max Group AF 0.84908313 (AMR)
Genomes Max Group AF 0.8245343 (EAS)
Exomes Max Group AF 0.85574519 (AMR)
ClinVar Allele:
23151
ClinVar RCV:
RCV000008580
ClinVar Variation:
8112
dbSNP:
4950928
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203186754G>C , CM000663.2:g.203186754G>C GRCh38
NC_000001.10:g.203155882G>C , CM000663.1:g.203155882G>C GRCh37
NC_000001.9:g.201422505G>C NCBI36
NG_013056.1:g.5041C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001276.2:c.-131C>G NP_001267.2:n.-131C>G
XM_011509105.1:c.-131C>G XP_011507407.1:n.-131C>G
XM_011509106.1:c.-131C>G XP_011507408.1:n.-131C>G
XM_011509107.1:c.-131C>G XP_011507409.1:n.-131C>G
XM_011509108.1:c.-131C>G XP_011507410.1:n.-131C>G
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