Canonical Allele Identifier: CA799753583

Gene:

Linked Data

• dbSNP Id: rs1481633768
• gnomAD v3: 4-89655922-A-G
• gnomAD v4: 4-89655922-A-G
• MyVariant Identifiers: chr4:g.90577073A>G (hg19) ; chr4:g.89655922A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89655922A>G , CM000666.2:g.89655922A>G	GRCh38
NC_000004.11:g.90577073A>G , CM000666.1:g.90577073A>G	GRCh37
NC_000004.10:g.90796096A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.434+28005A>G
XR_938987.1:n.688+28005A>G
XR_938988.1:n.554+28005A>G
XR_938990.1:n.299-35363A>G
XR_938991.1:n.434+28005A>G
XR_938994.1:n.779+28005A>G
XR_938995.1:n.613+28005A>G
XR_938986.2:n.459+28005A>G
XR_938987.2:n.748+28005A>G