Canonical Allele Identifier: CA830248028

Gene:

Linked Data

• dbSNP Id: rs1338909148
• gnomAD v3: 6-98048010-A-G
• gnomAD v4: 6-98048010-A-G
• MyVariant Identifiers: chr6:g.98495886A>G (hg19) ; chr6:g.98048010A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98048010A>G , CM000668.2:g.98048010A>G	GRCh38
NC_000006.11:g.98495886A>G , CM000668.1:g.98495886A>G	GRCh37
NC_000006.10:g.98602607A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_245563.2:n.372-51176A>G
XR_942809.1:n.372-51176A>G