Canonical Allele Identifier: CA146853385

Gene:

Linked Data

• dbSNP Id: rs999134589
• gnomAD v2: 6-122158206-T-A
• gnomAD v3: 6-121837060-T-A
• gnomAD v4: 6-121837060-T-A
• MyVariant Identifiers: chr6:g.122158206T>A (hg19) ; chr6:g.121837060T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.121837060T>A , CM000668.2:g.121837060T>A	GRCh38
NC_000006.11:g.122158206T>A , CM000668.1:g.122158206T>A	GRCh37
NC_000006.10:g.122199905T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_942936.1:n.241-20851T>A
XR_942937.1:n.240+69445T>A
XR_942938.1:n.241-20851T>A
XR_942939.1:n.241-20851T>A
XR_942940.1:n.241-20851T>A
XR_942941.1:n.241-20851T>A
XR_942936.2:n.241-20851T>A
XR_942937.3:n.240+69445T>A