Canonical Allele Identifier: CA2573428192
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523566T>G , CM000663.2:g.34523566T>G GRCh38
NC_000001.10:g.34989167T>G , CM000663.1:g.34989167T>G GRCh37
NC_000001.9:g.34761754T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947171.1:n.1073+24013A>C
XR_001737964.1:n.991+24013A>C