Canonical Allele Identifier: CA307575847

Gene:

Linked Data

• dbSNP Id: rs1016587237
• gnomAD v3: 19-33521944-G-T
• gnomAD v4: 19-33521944-G-T
• MyVariant Identifiers: chr19:g.34012850G>T (hg19) ; chr19:g.33521944G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521944G>T , CM000681.2:g.33521944G>T	GRCh38
NC_000019.9:g.34012850G>T , CM000681.1:g.34012850G>T	GRCh37
NC_000019.8:g.38704690G>T	NCBI36
NG_013358.1:g.4950C>A
NG_013358.2:g.4950C>A

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.3G>T
XR_001754035.2:n.11G>T
XR_935918.2:n.11G>T