Canonical Allele Identifier: CA571116539

Gene:

Linked Data

• dbSNP Id: rs1302407635
• gnomAD v2: 6-151954743-T-A
• gnomAD v3: 6-151633608-T-A
• gnomAD v4: 6-151633608-T-A
• MyVariant Identifiers: chr6:g.151954743T>A (hg19) ; chr6:g.151633608T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633608T>A , CM000668.2:g.151633608T>A	GRCh38
NC_000006.11:g.151954743T>A , CM000668.1:g.151954743T>A	GRCh37
NC_000006.10:g.151996436T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3626T>A