Canonical Allele Identifier: CA101489347
Gene:

Linked Data

dbSNP Id: rs1015435241
gnomAD v2: 4-90576938-C-G
gnomAD v3: 4-89655787-C-G
gnomAD v4: 4-89655787-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655787C>G , CM000666.2:g.89655787C>G GRCh38
NC_000004.11:g.90576938C>G , CM000666.1:g.90576938C>G GRCh37
NC_000004.10:g.90795961C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+27870C>G
XR_938987.1:n.688+27870C>G
XR_938988.1:n.554+27870C>G
XR_938990.1:n.299-35498C>G
XR_938991.1:n.434+27870C>G
XR_938994.1:n.779+27870C>G
XR_938995.1:n.613+27870C>G
XR_938986.2:n.459+27870C>G
XR_938987.2:n.748+27870C>G