Canonical Allele Identifier: CA154890285

Gene:

Linked Data

• dbSNP Id: rs895292744
• MyVariant Identifiers: chr7:g.17997450C>T (hg19) ; chr7:g.17957827C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17957827C>T , CM000669.2:g.17957827C>T	GRCh38
NC_000007.13:g.17997450C>T , CM000669.1:g.17997450C>T	GRCh37
NC_000007.12:g.17963975C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927078.1:n.271-843C>T