Canonical Allele Identifier: CA2526204360
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056920T>C , CM000665.2:g.53056920T>C GRCh38
NC_000003.11:g.53090936T>C , CM000665.1:g.53090936T>C GRCh37
NC_000003.10:g.53065976T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9681A>G
ENST00000607283.5:c.465-13666A>G
ENST00000607495.5:c.447+20768A>G