Canonical Allele Identifier: CA528155701

Gene: CHI3L1

Linked Data

• dbSNP Id: rs1362555942
• gnomAD v2: 1-203152719-A-G
• gnomAD v3: 1-203183591-A-G
• gnomAD v4: 1-203183591-A-G
• MyVariant Identifiers: chr1:g.203152719A>G (hg19) ; chr1:g.203183591A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203183591A>G , CM000663.2:g.203183591A>G	GRCh38
NC_000001.10:g.203152719A>G , CM000663.1:g.203152719A>G	GRCh37
NC_000001.9:g.201419342A>G	NCBI36
NG_013056.1:g.8204T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255409.8:c.465+50T>C MANE Select	ENSP00000255409.3:n.465+50T>C
ENST00000255409.7:c.465+50T>C	ENSP00000255409.3:n.465+50T>C
NM_001276.2:c.465+50T>C	NP_001267.2:n.465+50T>C
XM_011509105.1:c.483+50T>C	XP_011507407.1:n.483+50T>C
XM_011509106.1:c.483+50T>C	XP_011507408.1:n.483+50T>C
XM_011509107.1:c.465+50T>C	XP_011507409.1:n.465+50T>C
XM_011509108.1:c.483+50T>C	XP_011507410.1:n.483+50T>C
NM_001276.3:c.465+50T>C	NP_001267.2:n.465+50T>C
NM_001276.4:c.465+50T>C MANE Select	NP_001267.2:n.465+50T>C