Canonical Allele Identifier: CA35635713
Gene: CHI3L1 HGNC NCBI

Linked Data

dbSNP Id: rs970350429

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203183574G>A , CM000663.2:g.203183574G>A GRCh38
NC_000001.10:g.203152702G>A , CM000663.1:g.203152702G>A GRCh37
NC_000001.9:g.201419325G>A NCBI36
NG_013056.1:g.8221C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000255409.8:c.465+67C>T MANE Select ENSP00000255409.3:n.465+67C>T
ENST00000255409.7:c.465+67C>T ENSP00000255409.3:n.465+67C>T
NM_001276.2:c.465+67C>T NP_001267.2:n.465+67C>T
XM_011509105.1:c.483+67C>T XP_011507407.1:n.483+67C>T
XM_011509106.1:c.483+67C>T XP_011507408.1:n.483+67C>T
XM_011509107.1:c.465+67C>T XP_011507409.1:n.465+67C>T
XM_011509108.1:c.483+67C>T XP_011507410.1:n.483+67C>T
NM_001276.3:c.465+67C>T NP_001267.2:n.465+67C>T
NM_001276.4:c.465+67C>T MANE Select NP_001267.2:n.465+67C>T