Canonical Allele Identifier: CA818177326

Gene:

Linked Data

• dbSNP Id: rs1247271359
• gnomAD v3: 6-121837036-A-G
• gnomAD v4: 6-121837036-A-G
• MyVariant Identifiers: chr6:g.122158182A>G (hg19) ; chr6:g.121837036A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.121837036A>G , CM000668.2:g.121837036A>G	GRCh38
NC_000006.11:g.122158182A>G , CM000668.1:g.122158182A>G	GRCh37
NC_000006.10:g.122199881A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_942936.1:n.241-20875A>G
XR_942937.1:n.240+69421A>G
XR_942938.1:n.241-20875A>G
XR_942939.1:n.241-20875A>G
XR_942940.1:n.241-20875A>G
XR_942941.1:n.241-20875A>G
XR_942936.2:n.241-20875A>G
XR_942937.3:n.240+69421A>G