Canonical Allele Identifier: CA2502617074
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649537A>G , CM000666.2:g.148649537A>G GRCh38
NC_000004.11:g.149570689A>G , CM000666.1:g.149570689A>G GRCh37
NC_000004.10:g.149790139A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30669T>C
XR_001741441.1:n.1745+104953A>G
XR_939336.3:n.2921-30669T>C