Canonical Allele Identifier: CA566344778

Gene:

Linked Data

• gnomAD v2: 6-31407918-C-T
• MyVariant Identifiers: chr6:g.31407918C>T (hg19) ; chr6:g.31440141C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31440141C>T , CM000668.2:g.31440141C>T	GRCh38
NC_000006.11:g.31407918C>T , CM000668.1:g.31407918C>T	GRCh37
NC_000006.10:g.31515897C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.55-89G>A