Canonical Allele Identifier: CA765712721

Gene: CCL20

Linked Data

• dbSNP Id: rs10175070
• MyVariant Identifiers: chr2:g.228670575G>C (hg19) ; chr2:g.227805859G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227805859G>C , CM000664.2:g.227805859G>C	GRCh38
NC_000002.11:g.228670575G>C , CM000664.1:g.228670575G>C	GRCh37
NC_000002.10:g.228378819G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000646475.1:c.-201G>C	ENSP00000496658.1:n.-201G>C