Canonical Allele Identifier: CA101482582

Gene:

Linked Data

• dbSNP Id: rs981225051
• gnomAD v3: 4-89598088-T-C
• gnomAD v4: 4-89598088-T-C
• MyVariant Identifiers: chr4:g.90519239T>C (hg19) ; chr4:g.89598088T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89598088T>C , CM000666.2:g.89598088T>C	GRCh38
NC_000004.11:g.90519239T>C , CM000666.1:g.90519239T>C	GRCh37
NC_000004.10:g.90738262T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.298+10148T>C
XR_938987.1:n.433-65T>C
XR_938988.1:n.299-65T>C
XR_938990.1:n.298+10148T>C
XR_938991.1:n.298+10148T>C
XR_938992.1:n.298+10148T>C
XR_938994.1:n.643+10148T>C
XR_938995.1:n.477+10148T>C
XR_938996.1:n.298+10148T>C
XR_938997.1:n.298+10148T>C
XR_938986.2:n.323+10148T>C
XR_938987.2:n.493-65T>C