Canonical Allele Identifier: CA495615729

Gene:

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56957357G>C , CM000678.2:g.56957357G>C	GRCh38
NC_000016.9:g.56991269G>C , CM000678.1:g.56991269G>C	GRCh37
NC_000016.8:g.55548770G>C	NCBI36
NG_008952.1:g.435G>C