Canonical Allele Identifier: CA553236595

Gene:

Linked Data

• dbSNP Id: rs1257446363
• gnomAD v2: 4-90576843-T-A
• MyVariant Identifiers: chr4:g.90576843T>A (hg19) ; chr4:g.89655692T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89655692T>A , CM000666.2:g.89655692T>A	GRCh38
NC_000004.11:g.90576843T>A , CM000666.1:g.90576843T>A	GRCh37
NC_000004.10:g.90795866T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.434+27775T>A
XR_938987.1:n.688+27775T>A
XR_938988.1:n.554+27775T>A
XR_938990.1:n.299-35593T>A
XR_938991.1:n.434+27775T>A
XR_938994.1:n.779+27775T>A
XR_938995.1:n.613+27775T>A
XR_938986.2:n.459+27775T>A
XR_938987.2:n.748+27775T>A