Canonical Allele Identifier: CA553236597
Gene:

Linked Data

dbSNP Id: rs1474473010
gnomAD v2: 4-90576854-A-G
gnomAD v3: 4-89655703-A-G
gnomAD v4: 4-89655703-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655703A>G , CM000666.2:g.89655703A>G GRCh38
NC_000004.11:g.90576854A>G , CM000666.1:g.90576854A>G GRCh37
NC_000004.10:g.90795877A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+27786A>G
XR_938987.1:n.688+27786A>G
XR_938988.1:n.554+27786A>G
XR_938990.1:n.299-35582A>G
XR_938991.1:n.434+27786A>G
XR_938994.1:n.779+27786A>G
XR_938995.1:n.613+27786A>G
XR_938986.2:n.459+27786A>G
XR_938987.2:n.748+27786A>G