Canonical Allele Identifier: CA528156753
Gene: CHI3L1 HGNC NCBI
dbSNP:
10399931
2100230426
gnomAD v2:
1:203156080 T / A
gnomAD v3:
1:203186952 T / A
gnomAD v4:
chr1-203186952-T-A
Joint Max Group AF 0.00001925 (AFR)
Genomes Max Group AF 0.00001925 (AFR)
MyVariant.info:
GRCh38 chr1:g.203186952T>A
GRCh37 chr1:g.203156080T>A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203186952T>A , CM000663.2:g.203186952T>A GRCh38
NC_000001.10:g.203156080T>A , CM000663.1:g.203156080T>A GRCh37
NC_000001.9:g.201422703T>A NCBI36
NG_013056.1:g.4843A>T

Transcript Alleles

HGVS Amino-acid Change
XM_011509105.1:c.-329A>T XP_011507407.1:n.-329A>T
XM_011509106.1:c.-329A>T XP_011507408.1:n.-329A>T
XM_011509108.1:c.-329A>T XP_011507410.1:n.-329A>T
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