Canonical Allele Identifier: CA1065242121
Gene:

Linked Data

dbSNP Id: rs1722649229
gnomAD v3: 4-89655811-C-G
gnomAD v4: 4-89655811-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655811C>G , CM000666.2:g.89655811C>G GRCh38
NC_000004.11:g.90576962C>G , CM000666.1:g.90576962C>G GRCh37
NC_000004.10:g.90795985C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+27894C>G
XR_938987.1:n.688+27894C>G
XR_938988.1:n.554+27894C>G
XR_938990.1:n.299-35474C>G
XR_938991.1:n.434+27894C>G
XR_938994.1:n.779+27894C>G
XR_938995.1:n.613+27894C>G
XR_938986.2:n.459+27894C>G
XR_938987.2:n.748+27894C>G