Canonical Allele Identifier: CA1320446156
Gene:

Linked Data

dbSNP Id: rs2077889032

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033199G>A , CM000664.2:g.200033199G>A GRCh38
NC_000002.11:g.200897922G>A , CM000664.1:g.200897922G>A GRCh37
NC_000002.10:g.200606167G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22303C>T