Canonical Allele Identifier: CA296576141

Gene:

Linked Data

• dbSNP Id: rs982548582
• gnomAD v2: 18-10382884-A-T
• gnomAD v3: 18-10382887-A-T
• gnomAD v4: 18-10382887-A-T
• MyVariant Identifiers: chr18:g.10382884A>T (hg19) ; chr18:g.10382887A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10382887A>T , CM000680.2:g.10382887A>T	GRCh38
NC_000018.9:g.10382884A>T , CM000680.1:g.10382884A>T	GRCh37
NC_000018.8:g.10372884A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935143.1:n.919+1534A>T