Canonical Allele Identifier: CA823882034

Gene:

Linked Data

• dbSNP Id: rs1325680627
• MyVariant Identifiers: chr6:g.31407858A>C (hg19) ; chr6:g.31440081A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31440081A>C , CM000668.2:g.31440081A>C	GRCh38
NC_000006.11:g.31407858A>C , CM000668.1:g.31407858A>C	GRCh37
NC_000006.10:g.31515837A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.55-29T>G