Canonical Allele Identifier: CA553243422
Gene:

Linked Data

dbSNP Id: rs1192425533
gnomAD v2: 4-90519165-G-A
gnomAD v3: 4-89598014-G-A
gnomAD v4: 4-89598014-G-A
MyVariant Identifiers: chr4:g.90519165G>A (hg19) chr4:g.89598014G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89598014G>A , CM000666.2:g.89598014G>A GRCh38
NC_000004.11:g.90519165G>A , CM000666.1:g.90519165G>A GRCh37
NC_000004.10:g.90738188G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+10074G>A
XR_938987.1:n.433-139G>A
XR_938988.1:n.299-139G>A
XR_938990.1:n.298+10074G>A
XR_938991.1:n.298+10074G>A
XR_938992.1:n.298+10074G>A
XR_938994.1:n.643+10074G>A
XR_938995.1:n.477+10074G>A
XR_938996.1:n.298+10074G>A
XR_938997.1:n.298+10074G>A
XR_938986.2:n.323+10074G>A
XR_938987.2:n.493-139G>A
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