Canonical Allele Identifier: CA1583203903
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132527285T>A , CM000667.2:g.132527285T>A GRCh38
NC_000005.9:g.131862977T>A , CM000667.1:g.131862977T>A GRCh37
NC_000005.8:g.131890876T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-168-31999T>A ENSP00000492349.2:n.-168-31999T>A
ENST00000638504.1:n.207-31999T>A
ENST00000638568.2:c.-310-29047T>A ENSP00000491158.2:n.-310-29047T>A
ENST00000639899.1:n.290-31999T>A
ENST00000640655.2:c.-168-31999T>A ENSP00000491596.2:n.-168-31999T>A