Canonical Allele Identifier: CA1103260383

Gene: CCL26

Linked Data

• dbSNP Id: rs1802777971
• gnomAD v3: 7-75769608-C-A
• gnomAD v4: 7-75769608-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75769608C>A , CM000669.2:g.75769608C>A	GRCh38
NC_000007.13:g.75398926C>A , CM000669.1:g.75398926C>A	GRCh37
NC_000007.12:g.75236862C>A	NCBI36
NG_015989.1:g.25139G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005180.9:c.*85G>T MANE Select	ENSP00000005180.4:n.*85G>T
ENST00000005180.8:c.*85G>T	ENSP00000005180.4:n.*85G>T
ENST00000394905.2:c.*85G>T	ENSP00000378365.2:n.*85G>T
NM_006072.4:c.*85G>T	NP_006063.1:n.*85G>T
XM_017011671.1:c.*85G>T	XP_016867160.1:n.*85G>T
XM_017011672.1:c.*85G>T	XP_016867161.1:n.*85G>T
NM_001371936.1:c.*85G>T	NP_001358865.1:n.*85G>T
NM_001371938.1:c.*85G>T MANE Select	NP_001358867.1:n.*85G>T