Canonical Allele Identifier: CA836257798

Gene:

Linked Data

• dbSNP Id: rs1272463454
• MyVariant Identifiers: chr7:g.17997578T>C (hg19) ; chr7:g.17957955T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17957955T>C , CM000669.2:g.17957955T>C	GRCh38
NC_000007.13:g.17997578T>C , CM000669.1:g.17997578T>C	GRCh37
NC_000007.12:g.17964103T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927078.1:n.271-715T>C