Canonical Allele Identifier: CA829017199

Gene:

Linked Data

• dbSNP Id: rs1430141736
• MyVariant Identifiers: chr6:g.8525329G>A (hg19) ; chr6:g.8525096G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.8525096G>A , CM000668.2:g.8525096G>A	GRCh38
NC_000006.11:g.8525329G>A , CM000668.1:g.8525329G>A	GRCh37
NC_000006.10:g.8470328G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038979.1:n.626-33489G>A
NR_038980.1:n.649-33489G>A