Canonical Allele Identifier: CA35635661
Gene: CHI3L1 HGNC NCBI

Linked Data

dbSNP Id: rs553626259

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203183505G>C , CM000663.2:g.203183505G>C GRCh38
NC_000001.10:g.203152633G>C , CM000663.1:g.203152633G>C GRCh37
NC_000001.9:g.201419256G>C NCBI36
NG_013056.1:g.8290C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000255409.8:c.465+136C>G MANE Select ENSP00000255409.3:n.465+136C>G
ENST00000255409.7:c.465+136C>G ENSP00000255409.3:n.465+136C>G
NM_001276.2:c.465+136C>G NP_001267.2:n.465+136C>G
XM_011509105.1:c.483+136C>G XP_011507407.1:n.483+136C>G
XM_011509106.1:c.483+136C>G XP_011507408.1:n.483+136C>G
XM_011509107.1:c.465+136C>G XP_011507409.1:n.465+136C>G
XM_011509108.1:c.483+136C>G XP_011507410.1:n.483+136C>G
NM_001276.3:c.465+136C>G NP_001267.2:n.465+136C>G
NM_001276.4:c.465+136C>G MANE Select NP_001267.2:n.465+136C>G