Canonical Allele Identifier: CA2503877182

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.195007043T>C , CM000664.2:g.195007043T>C	GRCh38
NC_000002.11:g.195871767T>C , CM000664.1:g.195871767T>C	GRCh37
NC_000002.10:g.195580012T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001739836.1:n.553+52392A>G