Canonical Allele Identifier: CA1095881564

Gene:

Linked Data

• dbSNP Id: rs934672920
• gnomAD v3: 6-151627243-A-C
• gnomAD v4: 6-151627243-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151627243A>C , CM000668.2:g.151627243A>C	GRCh38
NC_000006.11:g.151948378A>C , CM000668.1:g.151948378A>C	GRCh37
NC_000006.10:g.151990071A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943113.1:n.669A>C
XR_943115.1:n.669A>C