Canonical Allele Identifier: CA1116942103

Gene:

Linked Data

• dbSNP Id: rs1810401468
• gnomAD v3: 8-97269808-A-G
• gnomAD v4: 8-97269808-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269808A>G , CM000670.2:g.97269808A>G	GRCh38
NC_000008.10:g.98282036A>G , CM000670.1:g.98282036A>G	GRCh37
NC_000008.9:g.98351212A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125390.1:n.471+149262T>C