Canonical Allele Identifier: CA626487391

Gene:

Linked Data

• dbSNP Id: rs1271309494
• gnomAD v2: 17-48289266-A-T
• gnomAD v3: 17-50211905-A-T
• gnomAD v4: 17-50211905-A-T
• MyVariant Identifiers: chr17:g.48289266A>T (hg19) ; chr17:g.50211905A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50211905A>T , CM000679.2:g.50211905A>T	GRCh38
NC_000017.10:g.48289266A>T , CM000679.1:g.48289266A>T	GRCh37
NC_000017.9:g.45644265A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934838.1:n.43-1930A>T