Canonical Allele Identifier: CA1011314172
Gene: CHI3L1 HGNC NCBI

Linked Data

dbSNP Id: rs770634446
gnomAD v3: 1-203183594-C-T
gnomAD v4: 1-203183594-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203183594C>T , CM000663.2:g.203183594C>T GRCh38
NC_000001.10:g.203152722C>T , CM000663.1:g.203152722C>T GRCh37
NC_000001.9:g.201419345C>T NCBI36
NG_013056.1:g.8201G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000255409.8:c.465+47G>A MANE Select ENSP00000255409.3:n.465+47G>A
ENST00000255409.7:c.465+47G>A ENSP00000255409.3:n.465+47G>A
NM_001276.2:c.465+47G>A NP_001267.2:n.465+47G>A
XM_011509105.1:c.483+47G>A XP_011507407.1:n.483+47G>A
XM_011509106.1:c.483+47G>A XP_011507408.1:n.483+47G>A
XM_011509107.1:c.465+47G>A XP_011507409.1:n.465+47G>A
XM_011509108.1:c.483+47G>A XP_011507410.1:n.483+47G>A
NM_001276.3:c.465+47G>A NP_001267.2:n.465+47G>A
NM_001276.4:c.465+47G>A MANE Select NP_001267.2:n.465+47G>A
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