Canonical Allele Identifier: CA2481646274
Gene: CHI3L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203180945C>G , CM000663.2:g.203180945C>G GRCh38
NC_000001.10:g.203150073C>G , CM000663.1:g.203150073C>G GRCh37
NC_000001.9:g.201416696C>G NCBI36
NG_013056.1:g.10850G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000255409.8:c.711+217G>C MANE Select ENSP00000255409.3:n.711+217G>C
ENST00000255409.7:c.711+217G>C ENSP00000255409.3:n.711+217G>C
ENST00000404436.2:c.199+217G>C
ENST00000472064.1:n.235+217G>C
ENST00000473185.1:n.973+217G>C
NM_001276.2:c.711+217G>C NP_001267.2:n.711+217G>C
XM_011509105.1:c.729+217G>C XP_011507407.1:n.729+217G>C
XM_011509106.1:c.729+217G>C XP_011507408.1:n.729+217G>C
XM_011509107.1:c.711+217G>C XP_011507409.1:n.711+217G>C
XM_011509108.1:c.729+217G>C XP_011507410.1:n.729+217G>C
NM_001276.3:c.711+217G>C NP_001267.2:n.711+217G>C
NM_001276.4:c.711+217G>C MANE Select NP_001267.2:n.711+217G>C