Canonical Allele Identifier: CA292897729

Gene:

Linked Data

• dbSNP Id: rs968633085
• MyVariant Identifiers: chr17:g.61583667G>T (hg19) ; chr17:g.63506306G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63506306G>T , CM000679.2:g.63506306G>T	GRCh38
NC_000017.10:g.61583667G>T , CM000679.1:g.61583667G>T	GRCh37
NC_000017.9:g.58937399G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577647.2:c.1970-750G>T	ENSP00000464149.1:n.1970-750G>T