Canonical Allele Identifier: CA881625598

Gene:

Linked Data

• dbSNP Id: rs1414534651
• gnomAD v3: 19-33522114-G-A
• gnomAD v4: 19-33522114-G-A
• MyVariant Identifiers: chr19:g.34013020G>A (hg19) ; chr19:g.33522114G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33522114G>A , CM000681.2:g.33522114G>A	GRCh38
NC_000019.9:g.34013020G>A , CM000681.1:g.34013020G>A	GRCh37
NC_000019.8:g.38704860G>A	NCBI36
NG_013358.1:g.4780C>T
NG_013358.2:g.4780C>T

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.73+100G>A
XR_935919.1:n.72+96G>A
XR_001754035.2:n.81+100G>A
XR_935918.2:n.81+100G>A