Canonical Allele Identifier: CA2481647397
Gene: CHI3L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203183679C= , CM000663.2:g.203183679C= GRCh38
NC_000001.10:g.203152807C= , CM000663.1:g.203152807C= GRCh37
NC_000001.9:g.201419430C= NCBI36
NG_013056.1:g.8116G=

Transcript Alleles

HGVS Amino-acid change
ENST00000255409.8:c.427G= MANE Select ENSP00000255409.3:p.Gly143=
ENST00000255409.7:c.427G= ENSP00000255409.3:p.Gly143=
NM_001276.2:c.427G= NP_001267.2:p.Gly143=
XM_011509105.1:c.445G= XP_011507407.1:p.Gly149=
XM_011509106.1:c.445G= XP_011507408.1:p.Gly149=
XM_011509107.1:c.427G= XP_011507409.1:p.Gly143=
XM_011509108.1:c.445G= XP_011507410.1:p.Gly149=
NM_001276.3:c.427G= NP_001267.2:p.Gly143=
NM_001276.4:c.427G= MANE Select NP_001267.2:p.Gly143=