Canonical Allele Identifier: CA148460499

Gene:

Linked Data

• dbSNP Id: rs137946154
• gnomAD v2: 6-134719977-A-G
• gnomAD v3: 6-134398839-A-G
• gnomAD v4: 6-134398839-A-G
• MyVariant Identifiers: chr6:g.134719977A>G (hg19) ; chr6:g.134398839A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.134398839A>G , CM000668.2:g.134398839A>G	GRCh38
NC_000006.11:g.134719977A>G , CM000668.1:g.134719977A>G	GRCh37
NC_000006.10:g.134761670A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428023.2:n.23+110A>G