Canonical Allele Identifier: CA817273936

Gene: CCN6

Linked Data

• dbSNP Id: rs1447775626
• gnomAD v3: 6-112069745-T-G
• gnomAD v4: 6-112069745-T-G
• MyVariant Identifiers: chr6:g.112069745T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069745T>G , CM000668.2:g.112069745T>G	GRCh38
NC_000006.11:g.112390948T>G , CM000668.1:g.112390948T>G	GRCh37
NC_000006.10:g.112497641T>G	NCBI36
NG_011748.1:g.20671T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361714.5:c.*125T>G	ENSP00000354734.2:n.*125T>G
ENST00000368666.6:c.*125T>G	ENSP00000357655.3:n.*125T>G