Canonical Allele Identifier: CA289293231

Gene:

Linked Data

• dbSNP Id: rs905862491
• MyVariant Identifiers: chr17:g.30237077G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30237077G>C , CM000679.2:g.30237077G>C	GRCh38
NC_000017.10:g.28564095G>C , CM000679.1:g.28564095G>C	GRCh37
NC_000017.9:g.25588221G>C	NCBI36
NG_011747.2:g.3860C>G

Transcript Alleles

HGVS	Amino-acid change
XR_934654.1:n.165+7G>C
XR_001752824.1:n.280+7G>C