Canonical Allele Identifier: CA842279336
Gene: CCL26 HGNC NCBI

Linked Data

dbSNP Id: rs1404093091
gnomAD v4: 7-75769618-G-T
MyVariant Identifiers: chr7:g.75769618G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769618G>T , CM000669.2:g.75769618G>T GRCh38
NC_000007.13:g.75398936G>T , CM000669.1:g.75398936G>T GRCh37
NC_000007.12:g.75236872G>T NCBI36
NG_015989.1:g.25129C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000005180.9:c.*75C>A MANE Select ENSP00000005180.4:n.*75C>A
ENST00000005180.8:c.*75C>A ENSP00000005180.4:n.*75C>A
ENST00000394905.2:c.*75C>A ENSP00000378365.2:n.*75C>A
NM_006072.4:c.*75C>A NP_006063.1:n.*75C>A
XM_017011671.1:c.*75C>A XP_016867160.1:n.*75C>A
XM_017011672.1:c.*75C>A XP_016867161.1:n.*75C>A
NM_001371936.1:c.*75C>A NP_001358865.1:n.*75C>A
NM_001371938.1:c.*75C>A MANE Select NP_001358867.1:n.*75C>A
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