Canonical Allele Identifier: CA1103260400
Gene: CCL26 HGNC NCBI

Linked Data

dbSNP Id: rs1017090744
gnomAD v3: 7-75769622-C-T
gnomAD v4: 7-75769622-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769622C>T , CM000669.2:g.75769622C>T GRCh38
NC_000007.13:g.75398940C>T , CM000669.1:g.75398940C>T GRCh37
NC_000007.12:g.75236876C>T NCBI36
NG_015989.1:g.25125G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000005180.9:c.*71G>A MANE Select ENSP00000005180.4:n.*71G>A
ENST00000005180.8:c.*71G>A ENSP00000005180.4:n.*71G>A
ENST00000394905.2:c.*71G>A ENSP00000378365.2:n.*71G>A
NM_006072.4:c.*71G>A NP_006063.1:n.*71G>A
XM_017011671.1:c.*71G>A XP_016867160.1:n.*71G>A
XM_017011672.1:c.*71G>A XP_016867161.1:n.*71G>A
NM_001371936.1:c.*71G>A NP_001358865.1:n.*71G>A
NM_001371938.1:c.*71G>A MANE Select NP_001358867.1:n.*71G>A
Search 100 bp 5'
Search 100 bp 3'