Canonical Allele Identifier: CA64382870
Gene:

Linked Data

dbSNP Id: rs763679478

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033112G>A , CM000664.2:g.200033112G>A GRCh38
NC_000002.11:g.200897835G>A , CM000664.1:g.200897835G>A GRCh37
NC_000002.10:g.200606080G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22216C>T