Canonical Allele Identifier: CA2481647356
Gene: CHI3L1 HGNC NCBI

Linked Data

dbSNP Id: rs1655991277

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203183581A>G , CM000663.2:g.203183581A>G GRCh38
NC_000001.10:g.203152709A>G , CM000663.1:g.203152709A>G GRCh37
NC_000001.9:g.201419332A>G NCBI36
NG_013056.1:g.8214T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000255409.8:c.465+60T>C MANE Select ENSP00000255409.3:n.465+60T>C
ENST00000255409.7:c.465+60T>C ENSP00000255409.3:n.465+60T>C
NM_001276.2:c.465+60T>C NP_001267.2:n.465+60T>C
XM_011509105.1:c.483+60T>C XP_011507407.1:n.483+60T>C
XM_011509106.1:c.483+60T>C XP_011507408.1:n.483+60T>C
XM_011509107.1:c.465+60T>C XP_011507409.1:n.465+60T>C
XM_011509108.1:c.483+60T>C XP_011507410.1:n.483+60T>C
NM_001276.3:c.465+60T>C NP_001267.2:n.465+60T>C
NM_001276.4:c.465+60T>C MANE Select NP_001267.2:n.465+60T>C