Canonical Allele Identifier: CA1338779630
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.239765595T>C , CM000664.2:g.239765595T>C GRCh38
NC_000002.11:g.240687289T>C , CM000664.1:g.240687289T>C GRCh37
NC_000002.10:g.240352226T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037808.1:n.73+2663T>C