Canonical Allele Identifier: CA35639447
Gene: CHI3L1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.203186870G>T
GRCh37 chr1:g.203155998G>T
gnomAD v3:
1:203186870 G / T
gnomAD v4:
chr1-203186870-G-T
Joint Max Group AF 0.0015999 (AMR)
Genomes Max Group AF 0.00152251 (AMR)
Exomes Max Group AF 0.00139174 (AMR)
dbSNP:
10399805
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203186870G>T , CM000663.2:g.203186870G>T GRCh38
NC_000001.10:g.203155998G>T , CM000663.1:g.203155998G>T GRCh37
NC_000001.9:g.201422621G>T NCBI36
NG_013056.1:g.4925C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011509105.1:c.-247C>A XP_011507407.1:n.-247C>A
XM_011509106.1:c.-247C>A XP_011507408.1:n.-247C>A
XM_011509108.1:c.-247C>A XP_011507410.1:n.-247C>A
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