Canonical Allele Identifier: CA292897752

Gene:

Linked Data

• dbSNP Id: rs142592698
• gnomAD v2: 17-61583757-G-T
• gnomAD v3: 17-63506396-G-T
• gnomAD v4: 17-63506396-G-T
• MyVariant Identifiers: chr17:g.61583757G>T (hg19) ; chr17:g.63506396G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63506396G>T , CM000679.2:g.63506396G>T	GRCh38
NC_000017.10:g.61583757G>T , CM000679.1:g.61583757G>T	GRCh37
NC_000017.9:g.58937489G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000577647.2:c.1970-660G>T	ENSP00000464149.1:n.1970-660G>T