Canonical Allele Identifier: CA2683369082

Gene: CCL26

Linked Data

• gnomAD v4: 7-75769598-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75769598T>C , CM000669.2:g.75769598T>C	GRCh38
NC_000007.13:g.75398916T>C , CM000669.1:g.75398916T>C	GRCh37
NC_000007.12:g.75236852T>C	NCBI36
NG_015989.1:g.25149A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005180.9:c.*95A>G MANE Select	ENSP00000005180.4:n.*95A>G
ENST00000005180.8:c.*95A>G	ENSP00000005180.4:n.*95A>G
ENST00000394905.2:c.*95A>G	ENSP00000378365.2:n.*95A>G
NM_006072.4:c.*95A>G	NP_006063.1:n.*95A>G
XM_017011671.1:c.*95A>G	XP_016867160.1:n.*95A>G
XM_017011672.1:c.*95A>G	XP_016867161.1:n.*95A>G
NM_001371936.1:c.*95A>G	NP_001358865.1:n.*95A>G
NM_001371938.1:c.*95A>G MANE Select	NP_001358867.1:n.*95A>G