Canonical Allele Identifier: CA136859003

Gene:

Linked Data

• dbSNP Id: rs900093046
• MyVariant Identifiers: chr6:g.31407671A>C (hg19) ; chr6:g.31439894A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439894A>C , CM000668.2:g.31439894A>C	GRCh38
NC_000006.11:g.31407671A>C , CM000668.1:g.31407671A>C	GRCh37
NC_000006.10:g.31515650A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.213T>G