Canonical Allele Identifier: CA2502977287
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056893A>G , CM000665.2:g.53056893A>G GRCh38
NC_000003.11:g.53090909A>G , CM000665.1:g.53090909A>G GRCh37
NC_000003.10:g.53065949A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9654T>C
ENST00000607283.5:c.465-13639T>C
ENST00000607495.5:c.447+20795T>C