Canonical Allele Identifier: CA1118643437

Gene:

Linked Data

• dbSNP Id: rs1814951341
• gnomAD v3: 8-122396140-T-G
• gnomAD v4: 8-122396140-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122396140T>G , CM000670.2:g.122396140T>G	GRCh38
NC_000008.10:g.123408379T>G , CM000670.1:g.123408379T>G	GRCh37
NC_000008.9:g.123477560T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928599.1:n.152+3032A>C
XR_928599.3:n.152+3032A>C