Canonical Allele Identifier: CA1369169836
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428050A= , CM000665.2:g.61428050A= GRCh38
NC_000003.11:g.61413724A= , CM000665.1:g.61413724A= GRCh37
NC_000003.10:g.61388764A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.165-364T=
XR_940893.1:n.164+464T=
XR_001740725.1:n.202+464T=
XR_940892.2:n.203-364T=