Canonical Allele Identifier: CA1680251656

Gene: CCR6

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167120802G>C , CM000668.2:g.167120802G>C	GRCh38
NC_000006.11:g.167534290G>C , CM000668.1:g.167534290G>C	GRCh37
NC_000006.10:g.167454280G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-14132G>C
ENST00000705249.1:c.1066-15236G>C	ENSP00000516101.1:n.1066-15236G>C
ENST00000705250.1:c.844-15236G>C	ENSP00000516102.1:n.844-15236G>C
ENST00000705251.1:c.*713-15236G>C	ENSP00000516103.1:n.*713-15236G>C
ENST00000705252.1:c.*536-15236G>C	ENSP00000516104.1:n.*536-15236G>C
ENST00000705253.1:c.*536-15236G>C	ENSP00000516105.1:n.*536-15236G>C
ENST00000705254.1:c.673-15236G>C	ENSP00000516106.1:n.673-15236G>C
ENST00000705255.1:n.1692-15236G>C
ENST00000400926.5:c.-98+8788G>C	ENSP00000383715.2:n.-98+8788G>C
NM_004367.5:c.-98+8788G>C	NP_004358.2:n.-98+8788G>C
XR_943250.1:n.1793C>G
XR_943251.1:n.1793C>G
XR_001744467.2:n.1187+614C>G
XR_001744469.2:n.1117+684C>G
XR_943250.3:n.1560C>G
XR_943251.3:n.1801C>G
NM_004367.6:c.-98+8788G>C	NP_004358.2:n.-98+8788G>C