Canonical Allele Identifier: CA1475304927
Gene:

Linked Data

dbSNP Id: rs1722644834

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655650A>G , CM000666.2:g.89655650A>G GRCh38
NC_000004.11:g.90576801A>G , CM000666.1:g.90576801A>G GRCh37
NC_000004.10:g.90795824A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938986.1:n.434+27733A>G
XR_938987.1:n.688+27733A>G
XR_938988.1:n.554+27733A>G
XR_938990.1:n.299-35635A>G
XR_938991.1:n.434+27733A>G
XR_938994.1:n.779+27733A>G
XR_938995.1:n.613+27733A>G
XR_938986.2:n.459+27733A>G
XR_938987.2:n.748+27733A>G