Canonical Allele Identifier: CA112973402

Gene:

Linked Data

• dbSNP Id: rs900546357
• gnomAD v2: 5-1447786-T-C
• gnomAD v3: 5-1447671-T-C
• gnomAD v4: 5-1447671-T-C
• MyVariant Identifiers: chr5:g.1447786T>C (hg19) ; chr5:g.1447671T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1447671T>C , CM000667.2:g.1447671T>C	GRCh38
NC_000005.9:g.1447786T>C , CM000667.1:g.1447786T>C	GRCh37
NC_000005.8:g.1500786T>C	NCBI36
NG_015885.1:g.2758A>G