Canonical Allele Identifier: CA313629784

Gene:

Linked Data

• dbSNP Id: rs781123848
• gnomAD v2: 20-23642424-G-T
• gnomAD v3: 20-23661787-G-T
• gnomAD v4: 20-23661787-G-T
• MyVariant Identifiers: chr20:g.23642424G>T (hg19) ; chr20:g.23661787G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23661787G>T , CM000682.2:g.23661787G>T	GRCh38
NC_000020.10:g.23642424G>T , CM000682.1:g.23642424G>T	GRCh37
NC_000020.9:g.23590424G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001754712.1:n.280+137G>T