Canonical Allele Identifier: CA292897742

Gene:

Linked Data

• dbSNP Id: rs887459769
• gnomAD v3: 17-63506355-G-A
• gnomAD v4: 17-63506355-G-A
• MyVariant Identifiers: chr17:g.61583716G>A (hg19) ; chr17:g.63506355G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63506355G>A , CM000679.2:g.63506355G>A	GRCh38
NC_000017.10:g.61583716G>A , CM000679.1:g.61583716G>A	GRCh37
NC_000017.9:g.58937448G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577647.2:c.1970-701G>A	ENSP00000464149.1:n.1970-701G>A