Canonical Allele Identifier: CA101489348
Gene:

Linked Data

dbSNP Id: rs538695676
gnomAD v3: 4-89655802-G-T
gnomAD v4: 4-89655802-G-T
MyVariant Identifiers: chr4:g.90576953G>T (hg19) chr4:g.89655802G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655802G>T , CM000666.2:g.89655802G>T GRCh38
NC_000004.11:g.90576953G>T , CM000666.1:g.90576953G>T GRCh37
NC_000004.10:g.90795976G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+27885G>T
XR_938987.1:n.688+27885G>T
XR_938988.1:n.554+27885G>T
XR_938990.1:n.299-35483G>T
XR_938991.1:n.434+27885G>T
XR_938994.1:n.779+27885G>T
XR_938995.1:n.613+27885G>T
XR_938986.2:n.459+27885G>T
XR_938987.2:n.748+27885G>T
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