Canonical Allele Identifier: CA1804794160

Gene:

Linked Data

• dbSNP Id: rs1810397576

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269593G>C , CM000670.2:g.97269593G>C	GRCh38
NC_000008.10:g.98281821G>C , CM000670.1:g.98281821G>C	GRCh37
NC_000008.9:g.98350997G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125390.1:n.471+149477C>G