Canonical Allele Identifier: CA1096189929

Gene:

Linked Data

• dbSNP Id: rs1778929726
• gnomAD v3: 6-155817697-A-G
• gnomAD v4: 6-155817697-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155817697A>G , CM000668.2:g.155817697A>G	GRCh38
NC_000006.11:g.156138831A>G , CM000668.1:g.156138831A>G	GRCh37
NC_000006.10:g.156180523A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+24278A>G
XR_943146.1:n.552-3027T>C
XR_001744423.1:n.606-3027T>C
XR_001744424.1:n.79+24278A>G