Canonical Allele Identifier: CA12934160
Gene:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72194681A>G , CM000670.2:g.72194681A>G GRCh38
NC_000008.10:g.73106916A>G , CM000670.1:g.73106916A>G GRCh37
NC_000008.9:g.73269470A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929040.1:n.472A>G
XR_929040.2:n.1097A>G