Canonical Allele Identifier: CA988923684

Gene:

Linked Data

• dbSNP Id: rs2031435379
• gnomAD v3: 18-31756901-A-G
• gnomAD v4: 18-31756901-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756901A>G , CM000680.2:g.31756901A>G	GRCh38
NC_000018.9:g.29336864A>G , CM000680.1:g.29336864A>G	GRCh37
NC_000018.8:g.27590862A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5238A>G