Canonical Allele Identifier: CA1320446151
Gene:

Linked Data

dbSNP Id: rs2077888990

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033187G>A , CM000664.2:g.200033187G>A GRCh38
NC_000002.11:g.200897910G>A , CM000664.1:g.200897910G>A GRCh37
NC_000002.10:g.200606155G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22291C>T