Canonical Allele Identifier: CA101489345
Gene:

Linked Data

dbSNP Id: rs182047218
gnomAD v3: 4-89655777-G-A
gnomAD v4: 4-89655777-G-A
MyVariant Identifiers: chr4:g.90576928G>A (hg19) chr4:g.89655777G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655777G>A , CM000666.2:g.89655777G>A GRCh38
NC_000004.11:g.90576928G>A , CM000666.1:g.90576928G>A GRCh37
NC_000004.10:g.90795951G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+27860G>A
XR_938987.1:n.688+27860G>A
XR_938988.1:n.554+27860G>A
XR_938990.1:n.299-35508G>A
XR_938991.1:n.434+27860G>A
XR_938994.1:n.779+27860G>A
XR_938995.1:n.613+27860G>A
XR_938986.2:n.459+27860G>A
XR_938987.2:n.748+27860G>A
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