Canonical Allele Identifier: CA148460505

Gene:

Linked Data

• dbSNP Id: rs959003927
• gnomAD v3: 6-134398928-C-T
• gnomAD v4: 6-134398928-C-T
• MyVariant Identifiers: chr6:g.134720066C>T (hg19) ; chr6:g.134398928C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.134398928C>T , CM000668.2:g.134398928C>T	GRCh38
NC_000006.11:g.134720066C>T , CM000668.1:g.134720066C>T	GRCh37
NC_000006.10:g.134761759C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428023.2:n.23+199C>T